Novel engineered t cell receptors and immune therapy using the same

ABSTRACT

The present invention pertains to antigen recognizing constructs against COL6A3 antigens. The invention in particular provides novel engineered T cell receptor (TCR) based molecules which are selective and specific for the tumor expressing antigen COL6A3. The TCR of the invention, and COL6A3 antigen binding fragments derived therefrom, are of use for the diagnosis, treatment and prevention of COL6A3 expressing cancerous diseases. Further provided are nucleic acids encoding the antigen recognizing constructs of the invention, vectors comprising these nucleic acids, recombinant cells expressing the antigen recognizing constructs and pharmaceutical compositions comprising the compounds of the invention.

CROSS REFERENCE TO RELATED APPLICATIONS

This application is a continuation of U.S. application Ser. No. 16/180,980, filed 5 Nov. 2018, which claims the benefit of U.S. Provisional Application Ser. No. 62/582,202, filed 6 Nov. 2017, and German Patent Application No. 10 2017 125 888.4, filed 6 Nov. 2017, the content of each of these applications is herein incorporated by reference in their entirety. This application is related to PCT/EP2018/080176, filed 5 Nov. 2018, the content of which is incorporated herein by reference in its entirety.

REFERENCE TO SEQUENCE LISTING SUBMITTED AS A COMPLIANT ASCII TEXT FILE (.TXT)

Pursuant to the EFS-Web legal framework and 37 CFR §§ 1.821-825 (see MPEP § 2442.03(a)), a Sequence Listing in the form of an ASCII-compliant text file (entitled “Sequence_Listing_3000058-012002_ST25.txt” created on 26 Dec. 2019, and 66,603 bytes in size) is submitted concurrently with the instant application, and the entire contents of the Sequence Listing are incorporated herein by reference.

FIELD

The present invention pertains to antigen recognizing constructs against COL6A3 antigens. The invention in particular provides novel engineered T cell receptor (TCR) based molecules which are selective and specific for the tumor expressing antigen COL6A3. The TCR of the invention, and COL6A3 antigen binding fragments derived therefrom, are of use for the diagnosis, treatment and prevention of COL6A3 expressing cancerous diseases. Further provided are nucleic acids encoding the antigen recognizing constructs of the invention, vectors comprising these nucleic acids, recombinant cells expressing the antigen recognizing constructs and pharmaceutical compositions comprising the compounds of the invention.

BACKGROUND OF THE INVENTION

The collagens are a superfamily of proteins that play a role in maintaining the integrity of various tissues. Collagens are extracellular matrix proteins and have a triple-helical domain as their common structural element. Collagen VI is a major structural component of micro fibrils. The basic structural unit of collagen VI is a heterotrimer of the alpha 1(VI), alpha 2(VI), and alpha 3(VI) collagen chains. The alpha 1(VI) and alpha 2(VI) chains are encoded by the COL6A1 and COL6A2 genes, respectively. The protein encoded by the COL6A3 gene is the alpha 3 subunit of type VI collagen (alpha 3(VI) collagen chain) (Bertini et al., 2002 Eur. J. Paediatr. Neurol 6:193-8). COL6A3's gene expression was previously shown to be associated with the progression of breast cancer and was elevated in colon cancer (Smith M J, et al. “Analysis of differential gene expression in colorectal cancer and stroma using fluorescence-activated cell sorting purification” British journal of cancer. 2009; 100:1452-1464; Tilman G et al “Human periostin gene expression in normal tissues, tumors and melanoma: evidences for periostin production by both stromal and melanoma cells” Mol Cancer. 2007; 6:80) and as a prognosis marker of colorectal carcinoma (Qiao J et al. “Stroma derived COL6A3 is a potential prognosis marker of colorectal carcinoma revealed by quantitative proteomics” Oncotarget. 2015 Oct. 6; 6(30): 29929-29946). COL6A3 gene locates 2q37 in the human genome and contains 44 exons. The COL6A3 protein has 3177 amino acids and contains 12 Von Willebrand factor type A (vWA) domains, one fibronectin type 3 domain and one BPTI/Kunitz family of serine protease inhibitors (KU) domain.

Targets for T-cell based immunotherapy represent peptide epitopes derived from tumor-associated or tumor-specific proteins, which are presented by molecules of the major histocompatibility complex (MHC). These tumor associated antigens (TAAs) can be peptides derived from all protein classes, such as enzymes, receptors, transcription factors, etc. which are expressed and, as compared to unaltered cells of the same origin, usually up-regulated in cells of the respective tumor.

Specific elements of the cellular immune response are capable of selectively recognizing and destroying tumor cells. The isolation of tumor antigen-specific T cells from tumor-infiltrating cell populations or from peripheral blood suggests that such cells play an important role in natural immune defense against cancer. CD8-positive T cells in particular, which recognize class I molecules of the major histocompatibility complex (MHC)-bearing peptides of usually 8 to 10 amino acid residues derived from proteins or defective ribosomal products (DRiPs) located in the cytosol, play an important role in this response. The MHC-molecules of the human are also designated as human leukocyte-antigens (HLA).

A TCR is a heterodimeric cell surface protein of the immunoglobulin super-family, which is associated with invariant proteins of the CD3 complex involved in mediating signal transduction. TCRs exist as αβ and γδ heterodimers, which are structurally similar but have quite distinct anatomical locations and probably functions. The extracellular portion of native heterodimeric αβTCR consists of two polypeptide chains, each of which has a membrane-proximal constant domain, and a membrane-distal variable domain. Each of the constant and variable domains includes an intra-chain disulfide bond. The variable domains contain the highly polymorphic loops analogous to the complementarity determining regions (CDRs) of antibodies. The use of TCR gene therapy overcomes a number of current hurdles. It allows equipping patients' own T cells with desired specificities and generation of sufficient numbers of T cells in a short period of time, avoiding their exhaustion. The TCR will be transduced into central memory T cells or T cells with stem cell characteristics, which may ensure better persistence and function upon transfer. TCR-engineered T cells will be infused into cancer patients rendered lymphopenic by chemotherapy or irradiation, allowing efficient engraftment but inhibiting immune suppression.

While advances have been made in the development of molecular-targeting drugs for cancer therapy, there remains a need in the art to develop new anti-cancer agents that specifically target molecules highly specific to cancer cells. The present description addresses that need by providing novel engineered COL6A3 TCRs, respective recombinant TCR constructs, nucleic acids, vectors and host cells that specifically bind COL6A3 epitope(s) as disclosed; and methods of using such molecules in the treatment of cancer.

SUMMARY OF THE INVENTION

In a first aspect the object of the invention is solved by an antigen recognizing construct comprising a first domain comprising three complementary determining regions (CDRs) according to SEQ ID NOs: 5 (CDRa1), 6 (CDRa2), and 7 (CDRa3), and a second domain comprising three complementary determining regions (CDRs) according to SEQ ID NOs: 13 (CDRb1), 14 (CDRb2), and 15 (CDRb3), wherein at least one of said complementary determining regions is replaced with at least one sequence selected from the group of: a) SEQ ID NO: 26 (CDRa1-mut1), and SEQ ID NOs: 37 to 49 (CDRb1-mut1 to CDRb1-mut13), preferably SEQ ID NO: 40, and b) mutated sequences of SEQ ID NO: 26, and SEQ ID NOs: 37 to 49, preferably SEQ ID NO: 40, comprising conservative amino acid exchanges.

In another aspect, CDRa1 of an antigen recognizing construct may have at least about 25%, at least about 30%, at least about 35%, at least about 40%, at least about 45%, at least about 50%, at least about 55%, at least about 60%, at least 65%, at least about 70%, at least about 75%, at least about 80%, at least about 85%, at least about 90%, at least about 95%, at least about 96%, at least about 97%, at least about 98%, or at least about 99% identity with the amino acid sequence according to SEQ ID NO: 5.

In another aspect, CDRa2 of an antigen recognizing construct may have at least about 25%, at least about 30%, at least about 35%, at least about 40%, at least about 45%, at least about 50%, at least about 55%, at least about 60%, at least about 65%, at least about 70%, at least about 75%, at least about 80%, at least about 85%, at least about 90%, at least about 95%, at least about 96%, at least about 97%, at least about 98%, or at least about 99% identity with the amino acid sequence according to SEQ ID NO: 6.

In another aspect, CDRa3 of an antigen recognizing construct may have at least about 25%, at least about 30%, at least about 35%, at least about 40%, at least about 45%, at least about 50%, at least about 55%, at least about 60%, at least about 65%, at least about 70%, at least about 75%, at least about 80%, at least about 85%, at least about 90%, at least about 95%, at least about 96%, at least about 97%, at least about 98%, or at least about 99% identity with the amino acid sequence according to SEQ ID NO: 7.

In another aspect, CDRb1 of an antigen recognizing construct may have at least about 25%, at least about 30%, at least about 35%, at least about 40%, at least about 45%, at least about 50%, at least about 55%, at least about 60%, at least about 65%, at least about 70%, at least about 75%, at least about 80%, at least about 85%, at least about 90%, at least about 95%, at least about 96%, at least about 97%, at least about 98%, or at least about 99% identity with the amino acid sequence according to SEQ ID NO: 13.

In another aspect, CDRb2 of an antigen recognizing construct may have at least about 25%, at least about 30%, at least about 35%, at least about 40%, at least about 45%, at least about 50%, at least about 55%, at least about 60%, at least about 65%, at least about 70%, at least about 75%, at least about 80%, at least about 85%, at least about 90%, at least about 95%, at least about 96%, at least about 97%, at least about 98%, or at least about 99% identity with the amino acid sequence according to SEQ ID NO: 14.

In another aspect, CDRb3 of an antigen recognizing construct may have at least about 25%, at least about 30%, at least about 35%, at least about 40%, at least about 45%, at least about 50%, at least about 55%, at least about 60%, at least about 65%, at least about 70%, at least about 75%, at least about 80%, at least about 85%, at least about 90%, at least about 95%, at least about 96%, at least about 97%, at least about 98%, or at least about 99% identity with the amino acid sequence according to SEQ ID NO: 15.

In the context of the present invention, the inventors have identified improved engineered versions of the COL6A3 TCR R4P3F9 comprising mutated CDR1 sequences in the alpha and beta chain(s) that are improving stability, recognition and selectivity of the parental R4P3F9. These maturated TCR variants have been selected in a two-step method, wherein one step selects for stability and the second for affinity of the variants (see examples). While the inventive TCRs comprise mutated CDR1 regions, it is likely that CDR2 and or CDR3 can be mutated as well in order to increase binding affinity/specificity and/or selectivity and such mutated CDRs ideally could be included in the existing constructs.

The affinity maturation identified variants with considerably stronger binding activity towards HLA-A*02/COL6A3-peptide, while retaining or even improving specificity. Compared to the parental TCR C-1 (R4P3F9 TCR comprising wild type CDRs, see Table 5), all variants of the invention improved IFN-gamma release with higher levels reached already for lower peptide loading concentrations.

Within the variable domain, CDR1 and CDR2 are found in the variable (V) region of a polypeptide chain, and CDR3 includes some of V, all of diversity (D) and joining (J) regions. It is assumed that CDR3 is the most variable and is the main CDR responsible for specifically and selectively recognizing an antigen. Surprisingly, for some TCRs CDR1 seems also to make contacts to the peptide and thus is also responsible for selective recognition. In the present case, without being bound to a specific theory, the mutated CDR1b seems to interact with position 8 of the COL6A3-peptide.

Native alpha-beta heterodimeric TCRs have an alpha chain and a beta chain. Each alpha chain comprises variable, joining and constant regions, and the beta chain also usually contains a short diversity region between the variable and joining regions, but this diversity region is often considered as part of the joining region. Each variable region comprises three CDRs (Complementarity Determining Regions) embedded in a framework sequence, one being the hypervariable region named CDR3. There are several types of alpha chain variable (Vα) regions and several types of beta chain variable (Vβ) regions distinguished by their framework, CDR1 and CDR2 sequences, and by a partly defined CDR3 sequence. The Vα types are referred to in IMGT nomenclature by a unique TRAV number, Vβ types are referred to by a unique TRBV number.

Preferably, an antigen recognizing construct of the invention comprises the respective CDR1 to CDR3 of one individual herein disclosed engineered TCR variable region of the invention. Preferred are antigen recognizing constructs (e.g., αβ and γδ TCRs) of the invention which comprise at least one, preferably two, maturated CDR1 sequences.

The CDR-variants as disclosed herein—in particular the CDR1-variants—can be modified by the substitution of one or more residues at different, possibly selective, sites within the peptide chain, if not otherwise stated. Such substitutions are of a conservative nature where one amino acid is replaced by an amino acid of similar structure and characteristics, such as where a hydrophobic amino acid is replaced by another hydrophobic amino acid. Even more conservative would be replacement of amino acids of the same or similar size and chemical nature, such as where leucine is replaced by isoleucine. In studies of sequence variations in families of naturally occurring homologous proteins, certain amino acid substitutions are more often tolerated than others, and these are often show correlation with similarities in size, charge, polarity, and hydrophobicity between the original amino acid and its replacement, and such is the basis for defining “conservative substitutions”. Preferred conservative substitutions are herein defined as exchanges within one of the following five groups: Group 1—small aliphatic, nonpolar or slightly polar residues (Ala, Ser, Thr, Pro, Gly); Group 2—polar, negatively charged residues and their amides (Asp, Asn, Glu, Gln); Group 3—polar, positively charged residues (His, Arg, Lys); Group 4—large, aliphatic, nonpolar residues (Met, Leu, Ile, Val, Cys); and Group 5—large, aromatic residues (Phe, Tyr, Trp).

Less conservative substitutions might involve the replacement of one amino acid by another that has similar characteristics but is somewhat different in size, such as replacement of an alanine by an isoleucine residue.

The term “specificity” or “antigen specificity” or “specific for” a given antigen, as used herein means that the antigen recognizing construct can specifically bind to said antigen, preferably a COL6A3 antigen, more preferably with high avidity, when said antigen is presented by HLA, preferably HLA A2. For example, a TCR, as antigen recognizing construct, may be considered to have “antigenic specificity” for COL6A3 antigens, if T cells expressing the TCR in response to COL6A3 presenting HLA secrete at least about 200 pg/ml or more (e.g., 250 pg/ml or more, 300 pg/ml or more, 400 pg/ml or more, 500 pg/ml or more, 600 pg/ml or more, 700 pg/ml or more, 1000 pg ml or more, 2,000 pg/ml or more, 2,500 pg/ml or more, 5,000 pg/ml or more) of interferon γ (IFN-γ) upon co-culture with HLA A2 target cells pulsed with a low concentration of a COL6A3 antigen, such as the COL6A3 epitopes and antigens provided herein below (e.g., about 10-11 mol/l, 10-10 mol/l, 10-9 mol/l, 10-8 mol/l, 10-7 mol/l, 10-6 mol/l, 10-5 mol/l). Alternatively, or additionally, a TCR may be considered to have “antigenic specificity” for COL6A3, if T cells expressing the TCR secrete at least twice as much IFN-γ as the untransduced background level of IFN-γ upon co-culture with target cells pulsed with a low concentration of COL6A3 antigens. Such a “specificity” as described above can—for example—be analyzed with an ELISA.

In one alternative or additional embodiment of the invention, the antigen recognizing construct is stable, and capable of specifically and/or selectively binding to a COL6A3 antigen; preferably wherein the COL6A3 antigen is a protein epitope or peptide having an amino acid sequence shown in SEQ ID NO: 1 or a variant thereof, wherein the variant is an amino acid deletion, addition, insertion or substitution of not more than three, preferably two and most preferably not more than one amino acid position.

The term “selectivity” or “selective recognizing/binding” is understood to refer to the property of an antigen recognizing construct, such as a TCR or antibody, to selectively recognize or bind to preferably only one specific epitope and preferably shows no or substantially no cross-reactivity to another epitope. Preferably “selectivity” or “selective recognizing/binding” means that the antigen recognizing construct (e.g., a TCR) selectively recognizes or binds to preferably only one specific epitope and preferably shows no or substantially no cross-reactivity to another epitope, wherein said epitope is unique for one protein, such that the antigen recognizing construct shows no or substantially no cross-reactivity to another epitope and another protein.

The antigen recognizing construct according to the invention is preferably selected from an antibody, or derivative or fragment thereof, a bispecific molecule, or a T cell receptor (TCR), or a derivative or fragment thereof. A derivative or fragment of an antibody or TCR of the invention shall preferably retain the antigen binding/recognizing ability of the parent molecule, in particular its specificity and/or selectivity as explained above.

In an embodiment of the invention, the inventive engineered TCRs are able to recognize COL6A3 antigens in a major histocompatibility complex (MHC) class I-dependent manner. “MHC class I-dependent manner,” as used herein, means that the TCR elicits an immune response upon binding to COL6A3 peptide antigens within the context of an MHC class I molecule. The MHC class I molecule can be any MHC class I molecule known in the art, e.g., HLA-A molecules. In a preferred embodiment of the invention, the MHC class I molecule is an HLA-A2 molecule.

The invention provides both single chain antigen recognizing construct and double chain recognizing constructs, as well as other variant molecules. The invention in particular provides an engineered TCR as antigen recognizing construct, or fragment or derivative thereof. The engineered TCR preferably is of human origin, which is understood as being generated from a human TCR locus and therefore comprising human TCR sequences. Furthermore, the TCR of the invention is characterized as affinity maturated TCR, which is capable of specifically and selectively recognizing COL6A3 peptide antigen. Another embodiment of the invention additionally or alternatively provides the antigen recognizing construct described above, which induces an immune response, preferably wherein the immune response is characterized by an increase in interferon (IFN) γ levels.

TCRs of the invention may be provided as single chain α or β, or γ and δ, molecules, or alternatively as double chain constructs composed of both the α and β chain, or γ and δ chain.

Most preferably, in some additional embodiments, wherein the disclosure refers to antigen recognizing constructs comprising any one, two or all of the CDR1 to CDR3 regions of the herein disclosed engineered TCR chains (see table 1). Antigen recognizing constructs may be preferred, which comprise the natural or the engineered CDR sequence having three, two, and preferably only one, modified amino acid residues. A modified amino acid residue may be selected from an amino acid insertion, deletion or substitution. Most preferred is that the three, two, preferably one modified amino acid residue is the first or last amino acid residue of the respective CDR sequence. If the modification is a substitution then it is preferable in some embodiments that the substitution is a conservative amino acid substitution.

The inventive TCRs may further comprise a constant region derived from any suitable species, such as any mammal, e.g., human, rat, monkey, rabbit, donkey, or mouse. In an embodiment of the invention, the inventive TCRs further comprise a human constant region. In some preferred embodiments, the constant region of the TCR of the invention may be slightly modified, for example, by the introduction of heterologous sequences, preferably mouse sequences, which may increase TCR expression and stability. Also, further stabilizing mutations as known from the state of the art (e.g., DE 10 2016 123 893.7) may be introduced, such as replacement of unfavorable amino acids in the V regions and/or the introduction of a disulfide bridge between the TCR C domains and the removal of unpaired cysteine.

As used herein, the term “murine” or “human,” when referring to an antigen recognizing construct, or a TCR, or any component of a TCR described herein (e.g., complementarity determining region (CDR), variable region, constant region, α chain, and/or β chain), means a TCR (or component thereof), which is derived from a mouse or a human unrearranged TCR locus, respectively.

In an embodiment of the invention, chimeric TCR are provided, wherein the TCR chains comprise sequences from multiple species. Preferably, a TCR of the invention may comprise an α chain comprising a human variable region of an α chain and, for example, a murine constant region of a murine TCR α chain.

In one embodiment, the TCR of the invention is a human TCR comprising human variable regions according to the above embodiments and human constant regions.

The TCR of the invention may be provided as a single chain TCR (scTCR). A scTCR can comprise a polypeptide of a variable region of a first TCR chain (e.g., an alpha chain) and a polypeptide of an entire (full-length) second TCR chain (e.g., a beta chain), or vice versa. Furthermore, the scTCR can optionally comprise one or more linkers which join the two or more polypeptides together. The linker can be, for instance, a peptide, which joins together two single chains, as described herein. Also provided is such a scTCR of the invention, which is fused to a human cytokine, such as IL-2, IL-7 or IL-15.

The antigen recognizing construct according to the invention can also be provided in the form of a multimeric complex, comprising at least two scTCR molecules, wherein said scTCR molecules are each fused to at least one biotin moiety, and wherein said scTCRs are interconnected by biotin-streptavidin interaction to allow the formation of said multimeric complex. Similar approaches for the generation of multimeric TCR are also possible and included in this disclosure. Also provided are multimeric complexes of a higher order, comprising more than two scTCR of the invention.

For the purposes of the present invention, a TCR is a moiety having at least one TCR alpha or gamma and/or TCR beta or delta variable domain. Generally, they comprise both a TCR alpha variable domain and a TCR beta variable domain. They may be αβ heterodimers or may be in single chain format. For use in adoptive therapy, an αβ heterodimeric TCR may, for example, be transfected as full length chains having both cytoplasmic and transmembrane domains. If desired, an introduced disulfide bond between residues of the respective constant domains may be present.

In a preferred embodiment, the antigen recognizing construct is a human TCR, or fragment or derivative thereof. A human TCR or fragment or derivative thereof is a TCR, which comprises over 50% of the corresponding human TCR sequence. Preferably, only a small part of the TCR sequence is of artificial origin or derived from other species. It is known, however, that chimeric TCRs, e.g., derived from human origin with murine sequences in the constant domains, are advantageous. Particularly preferred are, therefore, TCRs in accordance with the present invention, which contains murine sequences in the extracellular part of their constant domains.

Thus, it is also preferred that the inventive antigen recognizing construct is able to recognize its peptide antigen in a human leucocyte antigen (HLA) dependent manner, preferably in an HLA-A02 dependent manner. The term “HLA dependent manner” in the context of the present invention means that the antigen recognizing construct binds to the antigen only in the event that the antigenic peptide is presented by said HLA.

The antigen recognizing construct in accordance with the invention in one embodiment preferably induces an immune response, preferably wherein the immune response is characterized by the increase in interferon (IFN) γ levels.

The term “polypeptide” as used herein includes oligopeptides and refers to a single chain of amino acids connected by one or more peptide bonds. With respect to the inventive polypeptides, the functional portion can be any portion comprising contiguous amino acids of the TCR (or functional variant thereof), of which it is a part, provided that the functional portion specifically binds to a COL6A3 antigen, preferably as disclosed herein in table 1. The term “functional portion” when used in reference to a TCR (or functional variant thereof) refers to any part or fragment of the TCR (or functional variant thereof) of the invention, which part or fragment retains the biological activity of the TCR (or functional variant thereof), of which it is a part (the parent TCR or parent functional variant thereof). Functional portions encompass, for example, those parts of a TCR (or functional variant thereof) that retain the ability to specifically bind to a COL6A3 antigen (in an HLA-A2-dependent manner), or detect, treat, or prevent cancer, to a similar extent, the same extent, or to a higher extent, as the parent TCR (or functional variant thereof).

The functional portion can comprise additional amino acids at the amino or carboxy terminus of the portion, or at both termini, in which additional amino acids are not found in the amino acid sequence of the parent TCR or functional variant thereof. Desirably, the additional amino acids do not interfere with the biological function of the functional portion, e.g., specifically binding to COL6A3 antigens; and/or having the ability to detect cancer, treat or prevent cancer, etc. More desirably, the additional amino acids enhance the biological activity, as compared to the biological activity of the parent TCR or functional variant thereof.

As already mentioned above, the binding functionality of the TCR of the invention may be provided in the framework of an antibody. The term “antibody” in its various grammatical forms is used herein to refer to immunoglobulin molecules and immunologically active portions of immunoglobulin molecules, i.e., molecules that contain an antigen-binding site or a paratope. Such molecules are also referred to as “antigen binding fragments” of immunoglobulin molecules. The invention further provides an antibody, or antigen binding portion thereof, which specifically binds to the antigens described herein. The antibody can be any type of immunoglobulin that is known in the art. For instance, the antibody can be of any isotype, e.g., IgA, IgD, IgE, IgG, IgM, etc. The antibody can be monoclonal or polyclonal. The antibody can be a naturally-occurring antibody, e.g., an antibody isolated and/or purified from a mammal, e.g., mouse, rabbit, goat, horse, chicken, hamster, human, etc. Alternatively, the antibody can be a genetically-engineered antibody, e.g., a humanized antibody or a chimeric antibody. The antibody can be in monomeric or polymeric form.

The invention also provides antigen binding portions of any of the antibodies described herein. The antigen binding portion can be any portion that has at least one antigen binding site, such as Fab, F(ab′)2, dsFv, scFv, diabodies, and triabodies. A single-chain variable region fragment (scFv) antibody fragment, which consists of a truncated Fab fragment comprising the variable (V) domain of an antibody heavy chain linked to a V domain of a light antibody chain via a synthetic peptide, can be generated using routine recombinant DNA technology techniques. Similarly, disulfide-stabilized variable region fragments (dsFv) can be prepared by recombinant DNA technology, antibody fragments of the invention, however, are not limited to these exemplary types of antibody fragments. Also, the antibody, or antigen binding portion thereof, can be modified to comprise a detectable label, such as, for instance, a radioisotope, a fluorophore (e.g., fluorescein isothiocyanate (FITC), phycoerythrin (PE)), an enzyme (e.g., alkaline phosphatase, horseradish peroxidase), and element particles (e.g., gold particles).

Suitable methods of making antibodies are known in the art. For instance, standard hybridoma methods are described in, e.g., Kohler and Milstein, Eur. J. Immunol, 5, 51 1-519 (1976), Harlow and Lane (eds.), Antibodies: A Laboratory Manual, CSH Press (1988), and C. A. Janeway et al. (eds.), Immunobiology, 8 Ed., Garland Publishing, New York, N.Y. (201 l)). Alternatively, other methods, such as EBV-hybridoma methods (Haskard and Archer, J. Immunol. Methods, 74(2), 361-67 (1984), and Roder et al, Methods Enzymol, 121, 140-67 (1986)), and bacteriophage vector expression systems (see, e.g., Huse et al., Science, 246, 1275-81 (1989)) are known in the art. Further, methods of producing antibodies in non-human animals are described in, e.g., U.S. Pat. Nos. 5,545,806, 5,569,825, and 5,714,352, and U.S. Patent Application Publication No. 2002/0197266.

Some embodiments of the invention also pertain to TCRs, or functional fragments and polypeptides thereof, which are soluble TCRs. As used herein, the term “soluble T-cell receptor” refers to single chain or heterodimeric truncated variants of native TCRs, which comprise at least the variable domains of the TCR α-chain and β-chain linked by a polypeptide linker (SEQ ID NOs: 22, 24, 25 and 27). Soluble variants of TCRs usually lack at least the transmembrane and cytosolic domains of the native protein; sometimes preferably such soluble constructs do not comprise any constant domain sequences. The soluble T-cell receptor constructs of the invention, in preferred embodiments, comprise constructs consisting of α- and β-chain variable domain sequences as provided herein, connected by a suitable linker sequence. The variable domain sequence (amino acid or nucleic acid) of the soluble TCR α-chain and β-chains may be identical to the corresponding sequences in a native TCR or may comprise variants of soluble TCR α-chain and β-chain variable domain sequences, as compared to the corresponding native TCR sequences. The term “soluble T-cell receptor” as used herein encompasses soluble TCRs with variant or non-variant soluble TCR α-chain and β-chain variable domain sequences. The variations may be in the framework and/or CDR regions of the soluble TCR α-chain and β-chain variable domain sequences and can include, but are not limited to, amino acid deletion, insertion, substitution mutations as well as changes to the nucleic acid sequence, which do not alter the amino acid sequence. Soluble TCR of the invention in any case retain or preferentially improve the binding functionality of their parental TCR molecules.

The above problem is further solved by a nucleic acid encoding for an antigen recognizing construct of the invention, or any of the aforementioned protein or polypeptide constructs. The nucleic acid preferably (a) has a strand encoding for an antigen recognizing construct according to the invention; (b) has a strand complementary to the strand in (a); or (c) has a strand that hybridizes under stringent conditions with a molecule as described in (a) or (b). Stringent conditions are known to the person of skill in the art, specifically from Sambrook et al, “Molecular Cloning”. In addition to that, the nucleic acid optionally has further sequences, which are necessary for expressing the nucleic acid sequence corresponding to the protein, specifically for expression in a mammalian/human cell. The nucleic acid used can be contained in a vector suitable for allowing expression of the nucleic acid sequence corresponding to the polypeptide in a cell. However, the nucleic acids can also be used to transform an antigen-presenting cell, which may not be restricted to classical antigen-presenting cells, such as dendritic cells, in such a way that they themselves produce the corresponding proteins on their cellular surface.

By “nucleic acid” as used herein includes “polynucleotide,” “oligonucleotide,” and “nucleic acid molecule,” and generally means a polymer of DNA or RNA, which can be single-stranded or double-stranded, synthesized or obtained (e.g., isolated and/or purified) from natural sources, which can contain natural, non-natural or altered nucleotides, and can contain a natural, non-natural or altered internucleotide linkage, such as a phosphoroamidate linkage or a phosphorothioate linkage, instead of the phosphodiester found between the nucleotides of an unmodified oligonucleotide.

Preferably, the nucleic acids of the invention are recombinant. As used herein, the term “recombinant” refers to (i) molecules that are constructed outside living cells by joining natural or synthetic nucleic acid segments to nucleic acid molecules that can replicate in a living cell, or (ii) molecules that result from the replication of those described in (i) above. For purposes herein, the replication can be in vitro replication or in vivo replication. The nucleic acid can comprise any nucleotide sequence, which encodes any of the TCRs, polypeptides, or proteins, or functional portions or functional variants thereof described herein.

Furthermore, the invention provides a vector comprising a nucleic acid in accordance to the invention as described above. Desirably, the vector is an expression vector or a recombinant expression vector. The term “recombinant expression vector” refers in context of the present invention to a nucleic acid construct that allows for the expression of an mRNA, protein or polypeptide in a suitable host cell. The recombinant expression vector of the invention can be any suitable recombinant expression vector and can be used to transform or transfect any suitable host. Suitable vectors include those designed for propagation and expansion or for expression or both, such as plasmids and viruses. Examples of animal expression vectors include pEUK-Cl, pMAM, and pMAMneo. Preferably, the recombinant expression vector is a viral vector, e.g., a retroviral vector. The recombinant expression vector comprises regulatory sequences, such as transcription and translation initiation and termination codons, which are specific to the type of host cell (e.g., bacterium, fungus, plant, or animal), into which the vector is to be introduced and in which the expression of the nucleic acid of the invention may be performed. Furthermore, the vector of the invention may include one or more marker genes, which allow for selection of transformed or transfected hosts. The recombinant expression vector can comprise a native or normative promoter operably linked to the nucleotide sequence encoding the constructs of the invention, or to the nucleotide sequence, which is complementary to or which hybridizes to the nucleotide sequence encoding the constructs of the invention. The selections of promoters include, e.g., strong, weak, inducible, tissue-specific and developmental-specific promoters. The promoter can be a non-viral promoter or a viral promoter. The inventive recombinant expression vectors can be designed for either transient expression, for stable expression, or for both. Also, the recombinant expression vectors can be made for constitutive expression or for inducible expression.

The invention also pertains to a host cell comprising an antigen recognizing construct in accordance with the invention. Specifically, the host cell of the invention comprises a nucleic acid, or a vector as described herein above. The host cell can be a eukaryotic cell, e.g., plant, animal, fungi, or algae, or can be a prokaryotic cell, e.g., bacteria or protozoa. The host cell can be a cultured cell or a primary cell, i.e., isolated directly from an organism, e.g., a human. The host cell can be an adherent cell or a suspended cell, i.e., a cell that grows in suspension. For purposes of producing a recombinant TCR, polypeptide, or protein, the host cell is preferably a mammalian cell, e.g., Chinese Hamster Ovary (CHO) cell. Most preferably, the host cell is a human cell. While the host cell can be of any cell type, can originate from any type of tissue, and can be of any developmental stage, the host cell preferably is a peripheral blood leukocyte (PBL) or a peripheral blood mononuclear cell (PBMC). More preferably, the host cell is a T cell. The T cell can be any T cell, such as a cultured T cell, e.g., a primary T cell, or a T cell from a cultured T cell line, e.g., Jurkat, SupT1, etc., or a T cell obtained from a mammal, preferably a T cell or T cell precursor from a human patient. If obtained from a mammal, the T cell can be obtained from numerous sources, including but not limited to blood, bone marrow, lymph node, the thymus, or other tissues or fluids. T cells can also be enriched for or purified. Preferably, the T cell is a human T cell. More preferably, the T cell is a T cell isolated from a human. The T cell can be any type of T cell and can be of any developmental stage, including but not limited to, CD4-positive and/or CD8-positive, CD4-positive helper T cells, e.g., Th1 and Th2 cells, CD8-positive T cells (e.g., cytotoxic T cells), tumor infiltrating cells (TILs), memory T cells, naive T cells, and the like. Preferably, the T cell is a CD8-positive T cell or a CD4-positive T cell.

Preferably, the host cell of the invention is a lymphocyte, preferably, a T lymphocyte, such as a CD4-positive or CD8-positive T-cell. The host cell furthermore preferably is a tumor reactive T cell specific for COL6A3 expressing tumor cells.

One further aspect of the present invention relates to the herein disclosed antigen recognizing constructs, nucleic acids, vectors, pharmaceutical compositions and/or host cell for use in medicine. The use in medicine in one preferred embodiment includes the use in the diagnosis, prevention and/or treatment of a tumor disease, such as a malignant or benign tumor disease. The tumor disease is, for example, a tumor disease characterized by the expression of COL6A3, in a cancer or tumor cell of said tumor disease.

With respect to the above mentioned medical applications of the antigen recognizing constructs and other materials derived therefrom, the to be treated and/or diagnosed cancer can be any cancer, including any of acute lymphocytic cancer, acute myeloid leukemia, alveolar rhabdomyosarcoma, bone cancer, brain cancer, breast cancer, cancer of the anus, anal canal, or anorectum, cancer of the eye, cancer of the intrahepatic bile duct, cancer of the joints, cancer of the neck, gallbladder, or pleura, cancer of the nose, nasal cavity, or middle ear, cancer of the oral cavity, cancer of the vagina, cancer of the vulva, chronic lymphocytic leukemia, chronic myeloid cancer, colon cancer, esophageal cancer, cervical cancer, gastrointestinal carcinoid tumor, glioma, Hodgkin lymphoma, hypopharynx cancer, kidney cancer, larynx cancer, liver cancer, lung cancer, malignant mesothelioma, melanoma, multiple myeloma, nasopharynx cancer, non-Hodgkin lymphoma, cancer of the oropharynx, ovarian cancer, cancer of the penis, pancreatic cancer, peritoneum, omentum, and mesentery cancer, pharynx cancer, prostate cancer, rectal cancer, renal cancer, skin cancer, small intestine cancer, soft tissue cancer, stomach cancer, testicular cancer, thyroid cancer, cancer of the uterus, ureter cancer, and urinary bladder cancer. A preferred cancer is cancer is cancer of the uterine cervix, oropharynx, anus, anal canal, anorectum, vagina, vulva, or penis. A particularly preferred cancer is a COL6A3 positive cancer, including gastrointestinal and gastric cancer.

The constructs, proteins, TCRs, antibodies, polypeptides and nucleic acids of the invention are in particular for use in immune therapy, preferably, in adoptive T cell therapy. The administration of the compounds of the invention can, for example, involve the infusion of T cells of the invention into said patient. Preferably, such T cells are autologous T cells of the patient and in vitro transduced with a nucleic acid or antigen recognizing construct of the present invention.

WO 2016/011210 discloses engineered cells for adoptive therapy, including NK cells and T cells, and compositions containing the cells, and methods for their administration to subjects. The cells can contain genetically engineered antigen receptors that specifically bind to antigens, such as chimeric antigen receptors (CARs) and costimulatory receptors.

The object of the invention is also solved by a method of manufacturing a COL6A3 specific antigen recognizing construct expressing cell line, comprising

-   a. providing a suitable host cell, -   b. providing a genetic construct comprising a coding sequence     encoding the antigen recognizing construct according to any of     claims 1 to 4, -   c. introducing said genetic construct into said suitable host cell,     and -   d. expressing said genetic construct by said suitable host cell.

The method may further comprise a step of cell surface presentation of said antigen recognizing construct on said suitable host cell.

In other preferred embodiments, the genetic construct is an expression construct comprising a promoter sequence operably linked to said coding sequence.

Preferably, said antigen recognizing construct is of mammalian origin, preferably of human origin. The preferred suitable host cell for use in the method of the invention is a mammalian cell, such as a human cell, in particular a human T lymphocyte. T cells for use in the invention are described in detail herein above.

Also encompassed by the invention are embodiments, wherein said antigen recognizing construct is a modified TCR, wherein said modification is the addition of functional domains, such as a label or a therapeutically active substance. Furthermore, encompassed are TCR having alternative domains, such as an alternative membrane anchor domain instead of the endogenous transmembrane region.

Desirably, the transfection system for introducing the genetic construct into said suitable host cell is a retroviral vector system. Such systems are well known to the skilled artisan.

Also comprised by the present invention is in one embodiment the additional method step of isolation and purification of the antigen recognizing construct from the cell and, optionally, the reconstitution of the translated antigen recognizing construct-fragments in a T-cell.

In an alternative aspect of the invention a T-cell is provided obtained or obtainable by a method for the production of a T cell receptor (TCR), which is specific for tumorous cells and has high avidity as described herein above. Such a T cell is depending on the host cell used in the method of the invention, for example, a human or non-human T-cell, preferably a human TCR.

The inventive TCRs, polypeptides, proteins, (including functional variants thereof), nucleic acids, recombinant expression vectors, host cells (including populations thereof), and antibodies (including antigen binding portions thereof), can be isolated and/or purified. The term “isolated” as used herein means having been removed from its natural environment. The term “purified” as used herein means having been increased in purity, wherein “purity” is a relative term, and not to be necessarily construed as absolute purity. For example, the purity can be at least about 50%, can be greater than 60%, 70% o, 80%, 90%, 95%, or can be 100%.

The inventive antigen recognizing constructs, TCRs, polypeptides, proteins (including functional variants thereof), nucleic acids, recombinant expression vectors, host cells (including populations thereof), and antibodies (including antigen binding portions thereof), all of which are collectively referred to as “inventive TCR materials” hereinafter, can be formulated into a composition, such as a pharmaceutical composition. In this regard, the invention provides a pharmaceutical composition comprising any of the antigen recognizing constructs, TCRs, polypeptides, proteins, functional portions, functional variants, nucleic acids, expression vectors, host cells (including populations thereof), and antibodies (including antigen binding portions thereof) described herein, and a pharmaceutically acceptable carrier, excipient and/or stabilizer. The inventive pharmaceutical compositions containing any of the inventive TCR materials can comprise more than one inventive TCR material, e.g., a polypeptide and a nucleic acid, or two or more different TCRs (including functional portions and functional variants thereof). Alternatively, the pharmaceutical composition can comprise an inventive TCR material in combination with another pharmaceutically active agent(s) or drug(s), such as chemotherapeutic agents, e.g., asparaginase, busulfan, carboplatin, cisplatin, daunorubicin, doxorubicin, fluorouracil, gemcitabine, hydroxyurea, methotrexate, paclitaxel, rituximab, vinblastine, vincristine, etc. Preferably, the carrier is a pharmaceutically acceptable carrier. With respect to pharmaceutical compositions, the carrier can be any of those conventionally used for the particular inventive TCR material under consideration. Such pharmaceutically acceptable carriers are well-known to those skilled in the art and are readily available to the public. It is preferred that the pharmaceutically acceptable carrier be one, which has no detrimental side effects or toxicity under the conditions of use.

Thus, also provided is a pharmaceutical composition, comprising any of the herein described products of the invention and TCR materials of the invention, specifically any proteins, nucleic acids or host cells. In a preferred embodiment the pharmaceutical composition is for immune therapy, preferably adoptive cell therapy.

Preferably, the inventive TCR material is administered by injection, e.g., intravenously. When the inventive TCR material is a host cell expressing the inventive TCR (or functional variant thereof), the pharmaceutically acceptable carrier for the cells for injection may include any isotonic carrier such as, for example, normal saline (about 0.90% w/v of NaCl in water, about 300 mOsm/L NaCl in water, or about 9.0 g NaCl per liter of water), NORMOSOL R electrolyte solution (Abbott, Chicago, Ill.), PLASMA-LYTE A (Baxter, Deerfield, Ill.), about 5% dextrose in water, or Ringer's lactate. In an embodiment, the pharmaceutically acceptable carrier is supplemented with human serum albumin.

For purposes of the invention, the amount or dose (e.g., numbers of cells when the inventive TCR material is one or more cells) of the inventive TCR material administered may be sufficient to affect, e.g., a therapeutic or prophylactic response, in the subject or animal over a reasonable time frame. For example, the dose of the inventive TCR material should be sufficient to bind to a cancer antigen, or detect, treat or prevent cancer in a period of from about 2 hours or longer, e.g., 12 to 24 or more hours, from the time of administration. In certain embodiments, the time period could be even longer. The dose will be determined by the efficacy of the particular inventive TCR material and the condition of the animal (e.g., human), as well as the body weight of the animal (e.g., human) to be treated.

It is contemplated that the inventive pharmaceutical compositions, TCRs (including functional variants thereof), polypeptides, proteins, nucleic acids, recombinant expression vectors, host cells, or populations of cells can be used in methods of treating or preventing cancer, or COL6A3-positive premalignancy. The inventive TCRs (and functional variants thereof) are believed to bind specifically to COL6A3 antigen, such that the TCR (or related inventive polypeptide or protein and functional variants thereof), when expressed by a cell, is able to mediate an immune response against a target cell expressing the COL6A3 antigens of the invention. In this regard, the invention provides a method of treating or preventing a condition, in particular cancer, in a mammal, comprising administering to the mammal any of the pharmaceutical compositions, antigen recognizing constructs, in particular TCRs (and functional variants thereof), polypeptides, or proteins described herein, any nucleic acid or recombinant expression vector comprising a nucleotide sequence encoding any of the TCRs (and functional variants thereof), polypeptides, proteins described herein, or any host cell or population of cells comprising a recombinant vector, which encodes any of the constructs of the invention (and functional variants thereof), polypeptides, or proteins described herein, in an amount effective to treat or prevent the condition in the mammal, wherein the condition is cancer, preferably COL6A3 positive cancer.

Examples of pharmaceutically acceptable carriers or diluents useful in the present invention include stabilizers such as SPGA, carbohydrates (e.g., sorbitol, mannitol, starch, sucrose, glucose, dextran), proteins such as albumin or casein, protein containing agents such as bovine serum or skimmed milk and buffers (e.g., phosphate buffer).

The terms “treat,” and “prevent” as well as words stemming therefrom, as used herein, do not necessarily imply 100% or complete treatment or prevention. Rather, there are varying degrees of treatment or prevention of which one of ordinary skill in the art recognizes as having a potential benefit or therapeutic effect. In this respect, the inventive methods can provide any amount of any level of treatment or prevention of a condition in a mammal. Furthermore, the treatment or prevention provided by the inventive method can include treatment or prevention of one or more conditions or symptoms of the condition, e.g., cancer, being treated or prevented. For example, treatment or prevention can include promoting the regression of a tumor. Also, for purposes herein, “prevention” can encompass delaying the onset of the condition, or a symptom or condition thereof.

The present invention also relates to a method of treating cancer comprising administering a TCR, a nucleic acid, or a host cell of the present description in combination with at least one chemotherapeutic agent and/or radiation therapy.

Also provided is a method of treating cancer in a subject in need thereof, comprising:

-   -   a) isolating a cell from said subject;     -   b) transforming the cell with at least one vector encoding an         antigen recognizing construct of the present invention to         produce a transformed cell;     -   c) expanding the transformed cell to produce a plurality of         transformed cells; and     -   d) administering the plurality of transformed cells to said         subject.

Also provided is a method of treating cancer in a subject in need thereof, comprising:

-   -   a) isolating a cell from a healthy donor;     -   b) transforming the cell with a vector encoding an antigen         recognizing construct of the present invention to produce a         transformed cell;     -   c) expanding the transformed cell to produce a plurality of         transformed cells; and     -   d) administering the plurality of transformed cells to said         subject.

Also provided is a method of detecting cancer in a biological sample comprising:

-   -   a) contacting the biological sample with an antigen recognizing         construct of the present description;     -   b) detecting binding of the antigen recognizing construct to the         biological sample.

In some embodiments, the method of detecting cancer is carried out in vitro, in vivo or in situ.

Also provided is a method of detecting the presence of a condition in a mammal. The method comprises (i) contacting a sample comprising one or more cells from the mammal with any of the inventive TCRs (and functional variants thereof), polypeptides, proteins, nucleic acids, recombinant expression vectors, host cells, populations of cells, antibodies, or antigen binding portions thereof, or pharmaceutical compositions described herein, thereby forming a complex, and (ii) detecting the complex, wherein detection of the complex is indicative of the presence of the condition in the mammal, wherein the condition is cancer, such as a COL6A3-positive malignancy.

With respect to the inventive method of detecting a condition in a mammal, the sample of cells can be a sample comprising whole cells, lysates thereof, or a fraction of the whole cell lysates, e.g., a nuclear or cytoplasmic fraction, a whole protein fraction, or a nucleic acid fraction.

For purposes of the inventive detecting method, the contacting can take place in vitro or in vivo with respect to the mammal. Preferably, the contacting is in vitro.

Also, detection of the complex can occur through any number of ways known in the art. For instance, the inventive antigen recognizing constructs (and functional variants thereof), polypeptides, proteins, nucleic acids, recombinant expression vectors, host cells, populations of cells, or antibodies or TCRs, or antigen binding portions thereof, described herein, can be labeled with a detectable label such as, for instance, a radioisotope, a fluorophore (e.g., fluorescein isothiocyanate (FITC), phycoerythrin (PE)), an enzyme (e.g., alkaline phosphatase, horseradish peroxidase), and element particles (e.g., gold particles).

For purposes of the inventive methods, wherein host cells or populations of cells are administered, the cells can be cells that are allogeneic or autologous to the mammal. Preferably, the cells are autologous to the mammal.

With respect to the above mentioned medical applications of the TCR material of the invention, the to be treated and/or diagnosed cancer can be any cancer, including any of acute lymphocytic cancer, acute myeloid leukemia, alveolar rhabdomyosarcoma, bone cancer, brain cancer, breast cancer, cancer of the anus, anal canal, or anorectum, cancer of the eye, cancer of the intrahepatic bile duct, cancer of the joints, cancer of the neck, gallbladder, or pleura, cancer of the nose, nasal cavity, or middle ear, cancer of the oral cavity, cancer of the vagina, cancer of the vulva, chronic lymphocytic leukemia, chronic myeloid cancer, colon cancer, esophageal cancer, cervical cancer, gastrointestinal carcinoid tumor, glioma, Hodgkin lymphoma, hypopharynx cancer, kidney cancer, larynx cancer, liver cancer, lung cancer, malignant mesothelioma, melanoma, multiple myeloma, nasopharynx cancer, non-Hodgkin lymphoma, cancer of the oropharynx, ovarian cancer, cancer of the penis, pancreatic cancer, peritoneum, omentum, and mesentery cancer, pharynx cancer, prostate cancer, rectal cancer, renal cancer, skin cancer, small intestine cancer, soft tissue cancer, stomach cancer, testicular cancer, thyroid cancer, cancer of the uterus, ureter cancer, and urinary bladder cancer. A preferred cancer is cancer of the uterine cervix, oropharynx, anus, anal canal, anorectum, vagina, vulva, or penis. A particularly preferred cancer is a COL6A3 positive cancer, such as gastrointestinal or gastric cancer.

In general, the invention provides a method for treating a subject suffering from a tumor or tumor disease comprising the administration of the antigen recognizing constructs, nucleic acids, vectors, pharmaceutical compositions and/or host cell as disclosed by the present invention. Preferably the subject is a subject in need of such a treatment. The subject in preferred embodiments is a mammalian subject, preferably a human patient, suffering from a tumor or tumor disease, which is COL6A3-positive.

BRIEF DESCRIPTION OF THE DRAWINGS

The patent or application file contains at least one drawing executed in color. Copies of this patent or patent application publication with color drawing(s) will be provided by the Office upon request and payment of the necessary fee.

The present invention will now be further described in the following examples with reference to the accompanying figures and sequences, nevertheless, without being limited thereto. For the purposes of the present invention, all references as cited herein are incorporated by reference in their entireties. In the Figures and Sequences:

FIG. 1 shows the conversion of a TCR into stabilized Vα/Vβ single-chain TCR (scTv) via yeast surface display. ScTv molecules displayed on the surface of transformed Saccharomyces cerevisiae EBY100 were stained with FITC-labeled anti-Vbeta1 antibody and PE-labeled HLA-A*02/COL6A3-002 tetramer. The unmodified scTv R4P3F9 (left panel, SEQ ID NO: 22) is compared to an scTv clone bearing single point mutations to stabilize the scTv scaffold (right panel), which was derived from the selection of a random mutation scTv library.

FIG. 2 shows scTv affinity maturation via yeast surface display. Stabilized scTv molecules with and without affinity maturated CDR1 beta were stained with HLA-A*02 tetramers containing COL6A3-002 (SEQ ID NO: 1) and counterstained with a mix of HLA-A*02 tetramers containing 9 peptides (SEQ ID NO: 28 to 36) with high sequence similarity to COL6A3-002. Stabilized scTv (SEQ ID NO 27) with non-maturated beta chain CDR1 sequence RSGDLS (SEQ ID NO: 13) is compared with scTv clones bearing the affinity maturated beta chain CDR1 sequences AMDHPY (SEQ ID NO: 40) and ARWHRN (SEQ ID NO: 39).

FIG. 3 shows size exclusion chromatography elution profiles of anti-CD3 Fab-scTv R4P3F9S fusion variants 75-1 to 75-25.

FIG. 4 shows the HLA-A*02/COL6A3-002 binding kinetics of anti-CD3 Fab-scTv R4P3F9S fusion variants 75-1 to 75-25 as measured by biolayer interferometry. Analyzed concentrations of HLA-A*02/COL6A3-002 are indicated.

FIG. 5 shows binding analysis of anti-CD3 Fab-scTv R4P3F9S fusion variants 75-1 to 75-25 as measured via biolayer interferometry (BLI). 1 μM of HLA-A*02 in complex with the indicated similar peptides was analyzed.

FIG. 6 shows a comparison of HLA-A*02/COL6A3-002 and HLA-A*02/COL6A1-001 (SEQ ID NO: 30) binding kinetics of different anti-CD3 Fab-scTv R4P3F9S fusion variants. Analyzed concentrations of Fab-scTv molecules are indicated.

FIG. 7 shows staining of maturated R4P3F9 TCR variant expressing human CD8⁺ T cells with PE-labeled HLA-A*02/COL6A3-002 tetramers. For control purpose, no TCR (Mock) or the 1G4 TCR specific for NYESO1-001 was expressed and staining with PE-labeled HLA-A*02/NYESO1-001 tetramers was used.

FIG. 8 shows IFN-gamma release of maturated R4P3F9 TCR variant expressing human CD8⁺ T cells in response to COL6A3-002. For control purpose, no TCR (mock) or the 1G4 TCR specific for NYESO1-001 was expressed. IFN-gamma release was determined by ELISA after co-culture of electroporated CD8⁺ T cells with T2 cells loaded with a serial dilution of COL6A3-002.

FIG. 9 shows IFN-gamma release of maturated R4P3F9 TCR variant expressing human CD8⁺ T cells in response to COL6A3-002 and different similar peptides. For control purpose, no TCR (mock) or the 1G4 TCR specific for NYESO1-001 was expressed. IFN-gamma release was determined by ELISA after co-culture of electroporated CD8⁺ T cells with T2 cells loaded with 10 μM of COL6A3-002 or similar peptides.

FIG. 10 shows staining of maturated R4P3F9 TCR variant expressing human CD8⁺ T cells with PE-labeled peptide-HLA-A*02 tetramers. For control purpose, no TCR (Mock) or the 1G4 TCR specific for NYESO1-001 was expressed and staining with PE-labeled HLA-A*02/NYESO1-001 tetramers was used.

FIG. 11 shows IFN-gamma release of maturated R4P3F9 TCR variant expressing human CD8⁺ T cells in response to COL6A3-002 or COL6A1-001. For control purpose, no TCR (mock) or the 1G4 TCR specific for NYESO1-001 was expressed. IFN-gamma release was determined by ELISA after co-culture of electroporated CD8⁺ T cells with T2 cells loaded with a serial dilution of COL6A3-002 or COL6A1-001.

FIG. 12 shows IFN-gamma release of primary human CD8⁺ T cells expressing R4P3F9 TCR variants upon co-culture with different tumor cell lines. SF539, SW982 and Hs840.T cells present the target peptide at different levels. MCF-7 cells do not present the target peptide. As controls, effector cells without exogenous TCR were analyzed along with cells with TCRs of interest. IFN-gamma release was determined by ELISA. * marks a data point that is out of scale.

TABLE 1 Peptide sequences of the invention (positions are according to IMGT numbering: (François  Ehrenmann, Patrice Duroux, Chantal Ginestoux; Protein displays:  human (Homo sapiens) TRAV; IMGT Repertoire. IMGT ® the international ImMunoGenetics information system ® w ww.imgt.org.;  Created: 16/03/2011. Version: 03/06/2016; François Ehrenmann, Patrice Duroux, Chantal Ginestoux; Protein displays: human  (Homo sapiens) TRBV; IMGT Repertoire. IMGT ®, the international ImMunoGenetics information system ® w ww.imgt.org.; Created: 16/03/2011. Version: 03/06/2016.) SEQ ID NO: Name Description Sequence  1 COL6A3-002 FLLDGSANV  2 R4P3F9 R4P3F9 TCR MKSLRVLLVILWLQLSWVWSQQKEVEQNSGPLSVPEGAIA alpha alpha SLNCTYSDRGSQSFFWYRQYSGKSPELIMFIYSNGDKEDG chain- RFTAQLNKASQYVSLLIRDSQPSDSATYLCAAYSGAGSYQ full LTFGKGTKLSVIPNIQNPDPAVYQLRDSKSSDKSVCLFTD length FDSQTNVSQSKDSDVYITDKTVLDMRSMDFKSNSAVAWSN KSDFACANAFNNSIIPEDTFFPSPESSCDVKLVEKSFETD TNLNFQNLSVIGFRILLLKVAGFNLLMTLRLWSS  3 R4P3F9 R4P3F9 TCR MKSLRVLLVILWLQLSWVWSQ alpha alpha leader chain- leader peptide  4 R4P3F9 R4P3F9 TCR QKEVEQNSGPLSVPEGAIASLNCTYSDRGSQSFFWYRQYS alpha alpha GKSPELIMFIYSNGDKEDGRFTAQLNKASQYVSLLIRDSQ variable chain- PSDSATYLCAAYSGAGSYQLTFGKGTKLSVIP variable domain  5 R4P3F9 R4P3F9 TCR DRGSQS CDRa1 alpha chain- CDR1  6 R4P3F9 R4P3F9 TCR IYSNGD CDRa2 alpha chain- CDR2  7 R4P3F9 R4P3F9 TCR CAAYSGAGSYQLT CDRa3 alpha chain- CDR3  8 R4P3F9- R4P3F9 TCR NIQNPDPAVYQLRDSKSSDKSVCLFTDFDSQTNVSQSKDS alpha alpha DVYITDKTVLDMRSMDFKSNSAVAWSNKSDFACANAFNNS constant chain- IIPEDTFFPSPESSCDVKLVEKSFETDTNLNFQNLSVIGF constant RILLLKVAGFNLLMTLRLWSS domain  9 R4P3F9- R4P3F9 TCR NIQN alpha alpha constant chain- start constant domain start 10 R4P3F9 R4P3F9 TCR MGFRLLCCVAFCLLGAGPVDSGVTQTPKHLITATGQRVTL beta beta RCSPRSGDLSVYWYQQSLDQGLQFLIQYYNGEERAKGNIL chain- ERFSAQQFPDLHSELNLSSLELGDSALYFCASSVESSYGY full TFGSGTRLTVVEDLNKVFPPEVAVFEPSEAEISHTQKATL length VCLATGFFPDHVELSWWVNGKEVHSGVSTDPQPLKEQPAL NDSRYCLSSRLRVSATFWQNPRNHFRCQVQFYGLSENDEW TQDRAKPVTQIVSAEAWGRADCGFTSVSYQQGVLSATILY EILLGKATLYAVLVSALVLMAMVKRKDF 11 R4P3F9 R4P3F9 TCR MGFRLLCCVAFCLLGAGPV beta beta leader chain- leader peptide 12 R4P3F9 R4P3F9 TCR DSGVTQTPKHLITATGQRVTLRCSPRSGDLSVYWYQQSLD beta beta QGLQFLIQYYNGEERAKGNILERFSAQQFPDLHSELNLSS variable chain- LELGDSALYFCASSVESSYGYTFGSGTRLTVV variable domain 13 R4P3F9 R4P3F9 TCR RSGDLS CDRb1 beta chain- CDR1 14 R4P3F9 R4P3F9 TCR YYNGEE CDRb2 beta chain- CDR2 15 R4P3F9 R4P3F9 TCR CASSVESSYGYT CDRb3 beta chain- CDR3 16 R4P3F9 R4P3F9 TCR EDLNKVFPPEVAVFEPSEAEISHTQKATLVCLATGFFPDH beta beta VELSWWVNGKEVHSGVSTDPQPLKEQPALNDSRYCLSSRL constant chain- RVSATFWQNPRNHFRCQVQFYGLSENDEWTQDRAKPVTQI constant VSAEAWGRADCGFTSVSYQQGVLSATILYEILLGKATLYA domain VLVSALVLMAMVKRKDF 17 R4P3F9 R4P3F9 TCR EDLNK beta beta chain- constant constant start 1 domain start 1 18 R4P3F9 R4P3F9 TCR EDLKN beta beta chain- constant constant start 2 domain start 2 19 Aga2p- Aga2p MQLLRCFSIFSVIASVLAQELTTICEQIPSPTLESTPYSL R4P3F9 fusion STTTILANGKAMQGVFEYYKSVTFVSNCGSHPSTTSKGSP protein INTQYVFGGGGSDYKDDDDKGGGASQKEVEQNSGPLSVPE with scTv GAIASLNCTYSDRGSQSFFWYRQYSGKSPELIMSIYSNGD R4P3F9 and KEDGRFTAQLNKASQYVSLLIRDSQPSDSATYLCAAYSGA tags GSYQLTFGKGTKLSVIPNIQNGGGGSGGGGSGGGGSGGGG SGVTQTPKHLITATGQRVTLRCSPRSGDLSVYWYQQSLDQ GLQFLIQYYNGEERAKGNILERFSAQQFPDLHSELNLSSL ELGDSALYFCASSVESSYGYTFGSGTRLTVVEDLNKAAAG GSGGEQKLISEEDL 20 Aga2p Leader MQLLRCFSIFSVIASVLAQELTTICEQIPSPTLESTPYSL sequence STTTILANGKAMQGVFEYYKSVTFVSNCGSHPSTTSKGSP and Aga2p INTQYVF 21 FLAG tag FLAG tag GGGGSDYKDDDDKGGGAS plus linkers 22 scTv Single QKEVEQNSGPLSVPEGAIASLNCTYSDRGSQSFFWYRQYS R4P3F9 chain GKSPELIMSIYSNGDKEDGRFTAQLNKASQYVSLLIRDSQ variable PSDSATYLCAAYSGAGSYQLTFGKGTKLSVIPNIQNGGGG domains of SGGGGSGGGGSGGGGSGVTQTPKHLITATGQRVTLRCSPR R4P3F9 SGDLSVYWYQQSLDQGLQFLIQYYNGEERAKGNILERFSA with QQFPDLHSELNLSSLELGDSALYFCASSVESSYGYTFGSG linker; TRLTVVEDLNK aF55S in alpha variable domain 23 Myc tag Linker and AAAGGSGGEQKLISEEDL Myc tag 24 scTv scTv QKEVEQNSGPLSVPEGAIASLNCTYSDRGSQSFFWYRQYS R4P3F9- R4P3F9 GKSPELIMSIYSNGDKEDGRFTAQLNKASQYVSLLIRDSQ bQ43K with PSDSATYLCAAYSGAGSYQLTFGKGTKLSVIPNIQNGGGG stabilizing SGGGGSGGGGSGGGGSGVTQTPKHLITATGQRVTLRCSPR mutation SGDLSVYWYKQSLDQGLQFLIQYYNGEERAKGNILERFSA bQ43K in QQFPDLHSELNLSSLELGDSALYFCASSVESSYGYTFGSG beta TRLTVVEDLNK variable domain 25 scTv scTv QKEVEQNSGPLSVPEGAIASLNCTYSDRGSQSFFWYRQYS R4P3F9- R4P3F9 GKSPELIMSIYSNGDKEDGRFTAQLNKASQYVSLLIRDSQ bL72S with PSDSATYLCAAYSGAGSYQLTFGKGTKLSVIPNIQNGGGG stabilizing SGGGGSGGGGSGGGGSGVTQTPKHLITATGQRVTLRCSPR mutation SGDLSVYWYQQSLDQGLQFLIQYYNGEERAKGNISERFSA bL72S in QQFPDLHSELNLSSLELGDSALYFCASSVESSYGYTFGSG beta TRLTVVEDLNK variable domain 26 CDRa1 aG29R DRRSQS mutant1 mutation 27 scTv Stabilized QKEVEQNSGPLSVPEGAIASLNCTYSDRRSQSFFWYRQYS R4P3F9S version of GKSPELIMSIYSNGDKEDGRFTAQLNKASQYVSLLIRDSQ scTv PSDSATYLCAAYSGAGSYQLTFGKGTKLSVIPGGGGSGGG R4P3F9 GSGGGGSGGGGSGGGGSGVTQTPKHLITATGQRVTLRCSP RSGDLSVYWYKQSLDQGLQFLIQYYNGEERAKGNISERFS AQQFPDLHSELNLSSLELGDSALYFCASSVESSYGYTFGS GTRLTVV 28 AGRN-001 Similar ALLDGRVQL peptides 29 CLASP1-001 Similar RLLDGAFKL peptides 30 COL6A1-001 Similar ILLDGSASV peptides 31 COL6A2-001 Similar FLLDGSERL peptides 32 COL6A3-006 Similar FLFDGSANLV peptides 33 COL6A3-008 Similar FLFDGSANL peptides 34 COL6A3-014 Similar FLLDGSEGV peptides 35 VWA2-001 Similar FLLDGSNSV peptides 36 VWF-001 Similar FLLDGSSRL peptides 37 CDRb1 Beta chain- ARWHNN mutant 1 CDR1 variant 1 38 CDRb1 Beta chain- AKDHLN mutant 2 CDR1 variant 2 39 CDRb1 Beta chain- ARWHRN mutant 3 CDR1 variant 3 40 CDRb1 Beta chain- AMDHPY mutant 4 CDR1 variant 4 41 CDRb1 Beta chain- ATDHYN mutant 5 CDR1 variant 5 42 CDRb1 Beta chain- ARYHTN mutant 6 CDR1 variant 6 43 CDRb1 Beta chain- APYHLN mutant 7 CDR1 variant 7 44 CDRb1 Beta chain- AKDHTN mutant 8 CDR1 variant 8 45 CDRb1 Beta chain- ARYHRN mutant 9 CDR1 variant 9 46 CDRb1 Beta chain- ARWHSN mutant 10 CDR1 variant 10 47 CDRb1 Beta chain- ATDHYN mutant 11 CDR1 variant 11 48 CDRb1 Beta chain- RWGDLN mutant 12 CDR1 variant 12 49 CDRb1 Beta chain- ARDHLN mutant 13 CDR1 variant 13 50 75-1 Fab heavy MKWVTFISLLFLFSSAYSEVQLVESGGGLVQPGGSLRLSC chain with AASGYSFTGYTMNWVRQAPGKGLEWVALINPYKGVSTYNQ stabilized KFKDRFTISVDKSKNTAYLQMNSLRAEDTAVYYCARSGYY scTv GDSDWYFDVWGQGTLVTVSSASTKGPSVFPLAPSSKSTSG R4P3F9S GTAALGCLVKDYFPEPVTVSWNSGALTSGVHTFPAVLQSS GLYSLSSVVTVPSSSLGTQTYICNVNHKPSNTKVDKKVEP KSCDKTHTSPPSPAPPVAGQKEVEQNSGPLSVPEGAIASL NCTYSDRGSQSFFWYRQYSGKSPELIMSIYSNGDKEDGRF TAQLNKASQYVSLLIRDSQPSDSATYLCAAYSGAGSYQLT FGKGTKLSVIPNIQNGGGGSGGGGSGGGGSGGGGSGGGGS GVTQTPKHLITATGQRVTLRCSPRSGDLSVYWYKQSLDQG LQFLIQYYNGEERAKGNISERFSAQQFPDLHSELNLSSLE LGDSALYFCASSVESSYGYTFGSGTRLTVVEDLKN 51 75- Fab heavy MKWVTFISLLFLFSSAYSEVQLVESGGGLVQPGGSLRLSC Fab chain AASGYSFTGYTMNWVRQAPGKGLEWVALINPYKGVSTYNQ heavy KFKDRFTISVDKSKNTAYLQMNSLRAEDTAVYYCARSGYY chain GDSDWYFDVWGQGTLVTVSSASTKGPSVFPLAPSSKSTSG GTAALGCLVKDYFPEPVTVSWNSGALTSGVHTFPAVLQSS GLYSLSSVVTVPSSSLGTQTYICNVNHKPSNTKVDKKVEP KSCDKTHTSPPSPAPPVAG 52 75-  Fab light MKWVTFISLLFLFSSAYSDIQMTQSPSSLSASVGDRVTIT Fab chain CRASQDIRNYLNWYQQKPGKAPKLLIYYTSRLESGVPSRF light SGSGSGTDYTLTISSLQPEDFATYYCQQGNTLPWTFGQGT chain KVEIKRTVAAPSVFIFPPSDEQLKSGTASVVCLLNNFYPR EAKVQWKVDNALQSGNSQESVTEQDSKDSTYSLSSTLTLS KADYEKHKVYACEVTHQGLSSPVTKSFNRGEC 53 1G4 alpha 1G4 TCR METLLGLLILWLQLQWVSSKQEVTQIPAALSVPEGENLVL alpha NCSFTDSAIYNLQWFRQDPGKGLTSLLLIQSSQREQTSGR chain- LNASLDKSSGRSTLYIAASQPGDSATYLCAVRPTSGGSYI full PTFGRGTSLIVHPYIQNPDPAVYQLRDSKSSDKSVCLFTD length FDSQTNVSQSKDSDVYITDKTVLDMRSMDFKSNSAVAWSN KSDFACANAFNNSIIPEDTFFPSPESSCDVKLVEKSFETD TNLNFQNLSVIGFRILLLKVAGFNLLMTLRLWSS 54 1G4 alpha 1G4 TCR METLLGLLILWLQLQWVSSK leader alpha chain- leader peptide 55 1G4 alpha 1G4 TCR QEVTQIPAALSVPEGENLVLNCSFTDSAIYNLQWFRQDPG variable alpha KGLTSLLLIQSSQREQTSGRLNASLDKSSGRSTLYIAASQ chain- PGDSATYLCAVRPTSGGSYIPTFGRGTSLIVHP variable domain 56 1G4 alpha 1G4 TCR YIQNPDPAVYQLRDSKSSDKSVCLFTDFDSQTNVSQSKDS constant alpha DVYITDKTVLDMRSMDFKSNSAVAWSNKSDFACANAFNNS chain- IIPEDTFFPSPESSCDVKLVEKSFETDTNLNFQNLSVIGF constant RILLLKVAGFNLLMTLRLWSS domain 57 1G4 beta 1G4 TCR MSIGLLCCAALSLLWAGPVNAGVTQTPKFQVLKTGQSMTL beta chain- QCAQDMNHEYMSWYRQDPGMGLRLIHYSVGAGITDQGEVP full NGYNVSRSTTEDFPLRLLSAAPSQTSVYFCASSYVGNTGE length LFFGEGSRLTVLEDLKNVFPPEVAVFEPSEAEISHTQKAT LVCLATGFYPDHVELSWWVNGKEVHSGVSTDPQPLKEQPA LNDSRYCLSSRLRVSATFWQNPRNHFRCQVQFYGLSENDE WTQDRAKPVTQIVSAEAWGRADCGFTSESYQQGVLSATIL YEILLGKATLYAVLVSALVLMAMVKRKDSRG 58 1G4 beta 1G4 TCR MSIGLLCCAALSLLWAGPVNA leader beta chain- leader peptide 59 1G4 beta 1G4 TCR GVTQTPKFQVLKTGQSMTLQCAQDMNHEYMSWYRQDPGMG variable beta chain- LRLIHYSVGAGITDQGEVPNGYNVSRSTTEDFPLRLLSAA variable PSQTSVYFCASSYVGNTGELFFGEGSRLTVL domain 60 1G4 beta Beta chain- EDLKNVFPPEVAVFEPSEAEISHTQKATLVCLATGFYPDH constant constant VELSWWVNGKEVHSGVSTDPQPLKEQPALNDSRYCLSSRL domain RVSATFWQNPRNHFRCQVQFYGLSENDEWTQDRAKPVTQI VSAEAWGRADCGFTSESYQQGVLSATILYEILLGKATLYA VLVSALVLMAMVKRKDSRG 61 NYES01-001 Control SLLMWITQV peptide 62 C-14 C-14; C-5 MGFRLLCCVAFCLLGAGPVDSGVTQTPKHLITATGQRVTL beta; C-5 TCR full RCSPAMDHPYVYWYQQSLDQGLQFLIQYYNGEERAKGNIL beta length ERFSAQQFPDLHSELNLSSLELGDSALYFCASSVESSYGY beta chain TFGSGTRLTVVEDLNKVFPPEVAVFEPSEAEISHTQKATL with CDRb1 VCLATGFFPDHVELSWWVNGKEVHSGVSTDPQPLKEQPAL mutant 4 NDSRYCLSSRLRVSATFWQNPRNHFRCQVQFYGLSENDEW TQDRAKPVTQIVSAEAWGRADCGFTSVSYQQGVLSATILY EILLGKATLYAVLVSALVLMAMVKRKDF 63 C-14 C-14 TCR MKSLRVLLVILWLQLSWVWSQQKEVEQNSGPLSVPEGAIA alpha full SLNCTYSDRRSQSFFWYRQYSGKSPELIMFIYSNGDKEDG length RFTAQLNKASQYVSLLIRDSQPSDSATYLCAAYSGAGSYQ alpha LTFGKGTKLSVIPNIQNPDPAVYQLRDSKSSDKSVCLFTD chain with FDSQTNVSQSKDSDVYITDKTVLDMRSMDFKSNSAVAWSN CDRa1 KSDFACANAFNNSIIPEDTFFPSPESSCDVKLVEKSFETD mutant 1 TNLNFQNLSVIGFRILLLKVAGFNLLMTLRLWSS 64 75-5 Fab heavy MKWVTFISLLFLFSSAYSEVQLVESGGGLVQPGGSLRLSC chain with AASGYSFTGYTMNWVRQAPGKGLEWVALINPYKGVSTYNQ stabilized KFKDRFTISVDKSKNTAYLQMNSLRAEDTAVYYCARSGYY scTv GDSDWYFDVWGQGTLVTVSSASTKGPSVFPLAPSSKSTSG R4P3F9S GTAALGCLVKDYFPEPVTVSWNSGALTSGVHTFPAVLQSS and CDRb1 GLYSLSSVVTVPSSSLGTQTYICNVNHKPSNTKVDKKVEP mutant 4 KSCDKTHTSPPSPAPPVAGQKEVEQNSGPLSVPEGAIASL NCTYSDRGSQSFFWYRQYSGKSPELIMSIYSNGDKEDGRF TAQLNKASQYVSLLIRDSQPSDSATYLCAAYSGAGSYQLT FGKGTKLSVIPNIQNGGGGSGGGGSGGGGSGGGGSGGGGS GVTQTPKHLITATGQRVTLRCSPAMDHPYVYWYKQSLDQG LQFLIQYYNGEERAKGNISERFSAQQFPDLHSELNLSSLE LGDSALYFCASSVESSYGYTFGSGTRLTVVEDLKN 65 75-14 Fab heavy MKWVTFISLLFLFSSAYSEVQLVESGGGLVQPGGSLRLSC chain with AASGYSFTGYTMNWVRQAPGKGLEWVALINPYKGVSTYNQ stabilized KFKDRFTISVDKSKNTAYLQMNSLRAEDTAVYYCARSGYY scTv GDSDWYFDVWGQGTLVTVSSASTKGPSVFPLAPSSKSTSG R4P3F9S, GTAALGCLVKDYFPEPVTVSWNSGALTSGVHTFPAVLQSS CDRa1 GLYSLSSVVTVPSSSLGTQTYICNVNHKPSNTKVDKKVEP mutant 1 KSCDKTHTSPPSPAPPVAGQKEVEQNSGPLSVPEGAIASL and CDRb1 NCTYSDRRSQSFFWYRQYSGKSPELIMSIYSNGDKEDGRF mutant 4 TAQLNKASQYVSLLIRDSQPSDSATYLCAAYSGAGSYQLT FGKGTKLSVIPNIQNGGGGSGGGGSGGGGSGGGGSGGGGS GVTQTPKHLITATGQRVTLRCSPAMDHPYVYWYKQSLDQG LQFLIQYYNGEERAKGNISERFSAQQFPDLHSELNLSSLE LGDSALYFCASSVESSYGYTFGSGTRLTVVEDLKN 66 75-25 Fab heavy MKWVTFISLLFLFSSAYSEVQLVESGGGLVQPGGSLRLSC chain with AASGYSFTGYTMNWVRQAPGKGLEWVALINPYKGVSTYNQ stabilized KFKDRFTISVDKSKNTAYLQMNSLRAEDTAVYYCARSGYY scTv GDSDWYFDVWGQGTLVTVSSASTKGPSVFPLAPSSKSTSG R4P3F9S in GTAALGCLVKDYFPEPVTVSWNSGALTSGVHTFPAVLQSS beta/alpha GLYSLSSVVTVPSSSLGTQTYICNVNHKPSNTKVDKKVEP orientation, KSCDKTHTSPPSPAPPVAGGVTQTPKHLITATGQRVTLRC CDRa1 SPRSGDLSVYWYKQSLDQGLQFLIQYYNGEERAKGNISER mutant 1 FSAQQFPDLHSELNLSSLELGDSALYFCASSVESSYGYTF GSGTRLTVVEDLKNGGGGSGGGGSGGGGSGGGGSGGGGSQ KEVEQNSGPLSVPEGAIASLNCTYSDRRSQSFFWYRQYSG KSPELIMSIYSNGDKEDGRFTAQLNKASQYVSLLIRDSQP SDSATYLCAAYSGAGSYQLTFGKGTKLSVIPNIQN

EXAMPLES

Native T cell receptors (TCRs) against cancer antigens are often of lower affinity when compared to TCRs targeting viral antigens, and this may be one possible explanation for tumor immune escape (Aleksic et al. 2012). Therefore, it is desirable to have higher affinity TCR variants designed for the use as antigen recognizing constructs in an adoptive cell therapy, or as recognition module of a soluble approach, i.e., using bispecific molecules (Hickman et al. 2016). This invention thus relates to the modification and optimization of the naturally occurring T cell receptor R4P3F9 (SEQ ID NOs: 2 and 10) targeting the tumor associated peptide COL6A3-002 (SEQ ID NO: 1) with an affinity of about 60 μM (DE102016115246).

Example 1: Generation of Stable scTv

For the present invention, the previously investigated TCR R4P3F9 (SEQ ID NOs: 2 and 10) was converted into a single chain TCR construct (scTv, SEQ ID NO: 22) for maturation via yeast surface display by combination of the variable alpha (SEQ ID NO: 4) and beta (SEQ ID NO: 12) domain with appendages of the respective constant domains (SEQ ID NOs: 9 and 17) and an appropriate glycine-serine linker sequence. The DNA of the corresponding sequence was synthesized and transformed into Saccharomyces cerevisiae EB Y100 (MATa AGA1::GAL1AGA1::URA3 ura352 trp1 leu2delta200 his3delta200 pep4::HIS3 prbd1.6R can1 GAL) (ATCC® MYA 4941™) together with a yeast display vector containing a leader sequence and the Aga2p yeast mating protein (SEQ ID NO: 20), based on pCT302 (Boder et al. 2000). The resulting fusion protein after homologous recombination in the yeast (SEQ ID NO: 19) contains a leader peptide at the N-terminus of the Aga2p protein, responsible for the display of the protein of interest (Boder et al. 1997), short peptide tags including linker sequences (SEQ ID NOs: 21 and 23) for expression controls and the protein of interest, namely the scTv R4P3F9 (SEQ ID NO: 22) or its variants. The transformation was performed as described in DE102016121899 and resulted in up to 10⁹ yeast clones per library. The libraries were generated via a random mutation PCR approach spanning the whole gene sequence of the scTv R4P3F9.

The selection process for the yeast clones bearing the best expressing scTv that is selectively binding to COL6A3-002 in context of HLA-A*02 was essentially performed as described in Smith et al 2015. In order to ascertain high expression and correct conformation of the scTv R4P3F9 variant, displayed on the yeast surface, an anti-Vbeta1 (Beckman Coulter, clone BL37.2) antibody was used, together with HLA-A*02/COL6A3-002 tetramer (FIG. 1). The scTv conversion by yeast surface display revealed two crucial stabilizing mutations in the framework region together with the original CDR sequences for the proper presentation of the scTv on the cell surface, namely bQ43K (SEQ ID NO: 24) and bL72S (SEQ ID NO: 25), both located on the beta chain. Furthermore, during stability maturation position 29 in the CDR1 of the alpha chain (SEQ ID NO: 5) was converted from glycine to arginine (CDRa1 mutant 1, SEQ ID NO: 26), which resulted in improved tetramer binding.

Example 2: Affinity Maturation of Stabilized scTv

To generate scTv molecules with higher binding affinity towards HLA-A*02/COL6A3-002, the CDRb1 (SEQ ID NO: 13) was degenerated using the previously identified stabilized scTv R4P3F9S scaffold (SEQ ID NO: 27) expressing the stabilizing mutations aG29R, bQ43K and bL72S. The CDRb1 residues were randomized by using degenerate DNA oligo primers essentially as described previously (Smith et al. 2015). The resulting DNA library was transformed as described in example 1. To retain scTv binding selectivity, negative selection was employed against HLA-A*02 tetramers comprising peptides derived from normal tissues (SEQ ID NOs: 28 to 36), which show high sequence similarity to COL6A3-002 peptide.

For the selection of affinity enhanced and selective scTv R4P3F9S variants a decreasing concentration of HLA-A*02/COL6A3-002 tetramer was used for each sorting round. After three selection rounds, single scTv clones were isolated and sequenced, resulting in a variety of affinity maturated CDRb1 sequences (SEQ ID NOs: 37 to 49). For scTv with maturated CDRb1 sequences a strong improvement in COL6A3-002 binding could be demonstrated while the selectivity of COL6A3-002 binding was retained as no binding of 9 similar peptides was observed (FIG. 2).

Example 3: Production of Bispecific Antibody-scTv Fusion Proteins

Stabilized and affinity maturated scTv against HLA-A*02/COL6A3-002 can be expressed in fusion with an antibody moiety directed against CD3 allowing tumor-specific retargeting and activation of T cells independent of their natural specificity. The inventors generated bispecific antibody-TCR fusion proteins comprising an anti-CD3 Fab (UCHT1) heavy chain (SEQ ID NO: 51) fused to scTv R4P3F9S variants (SEQ ID NOs: 50, 64, 65 and 66) and an anti-CD3 Fab (UCHT1) light chain (SEQ ID NO: 52). The resulting Fab-scTv fusion proteins have a molecular mass of approximately 75 kDa. Based on different CDR1 sequences of the scTv R4P3F9S alpha (SEQ ID NOs: 5 and 26) and beta chain (SEQ ID NOs: 13 and 37 to 49) different Fab-scTv fusion variants (75-1 to 75-25, Table 2) were expressed in transiently transfected ExpiCHO cells as recommended by the manufacturer. Proteins were purified by protein L and size exclusion chromatography. All fusion variants could be produced with yields ranging from 80 μg up to 1 mg (Table 2) and homogeneously formed heterodimers at the expected size as analyzed by size exclusion chromatography (FIG. 3).

TABLE 2 Nomenclature and yields of bispecific Fab-scTv fusion proteins. The molecules are based on SEQ ID NOs 50 and 52 and the indicated CDRa1 and CDRb1 variants. Yield Variant CDRa1/SEQ CDRb1/SEQ [μg] 75-1 DRGSQS RSGDLS  267.9 (SEQ ID NO. 5) (SEQ ID NO. 13) 75-2 DRGSQS ARWHNN   78.4 (SEQ ID NO. 5) (SEQ ID NO. 37) 75-3 DRGSQS AKDHLN  646.7 (SEQ ID NO. 5) (SEQ ID NO. 38) 75-4 DRGSQS ARWHRN  704.3 (SEQ ID NO. 5) (SEQ ID NO. 39) 75-5 DRGSQS AMDHPY  397.2 (SEQ ID NO. 5) (SEQ ID NO. 40) 75-6 DRGSQS ATDHYN  268.1 (SEQ ID NO. 5) (SEQ ID NO. 41) 75-7 DRGSQS ARYHTN   83.2 (SEQ ID NO. 5) (SEQ ID NO. 42) 75-8 DRGSQS APYHLN  765.7 (SEQ ID NO. 5) (SEQ ID NO. 43) 75-9 DRGSQS AKDHTN 1067.2 (SEQ ID NO. 5) (SEQ ID NO. 44) 75-10 DRRSQS RSGDLS  389.6 (SEQ ID NO. 26) (SEQ ID NO. 13) 75-11 DRRSQS ARWHNN  270.4 (SEQ ID NO. 26) (SEQ ID NO. 37) 75-12 DRRSQS AKDHLN  943.6 (SEQ ID NO. 26) (SEQ ID NO. 38) 75-13 DRRSQS ARWHRN  560.3 (SEQ ID NO. 26) (SEQ ID NO. 39) 75-14 DRRSQS AMDHPY  360.7 (SEQ ID NO. 26) (SEQ ID NO. 40) 75-15 DRRSQS ATDHYN  541.5 (SEQ ID NO. 26) (SEQ ID NO. 41) 75-16 DRRSQS ARYHTN  403.6 (SEQ ID NO. 26) (SEQ ID NO. 42) 75-17 DRRSQS APYHLN  195.5 (SEQ ID NO. 26) (SEQ ID NO. 43) 75-18 DRRSQS AKDHTN  731.3 (SEQ ID NO. 26) (SEQ ID NO. 44) 75-19 DRRSQS ARYHRN  794   (SEQ ID NO. 26) (SEQ ID NO. 45) 75-20 DRRSQS ARWHSN   85.5 (SEQ ID NO. 26) (SEQ ID NO. 46) 75-21 DRRSQS ATDHYN  276   (SEQ ID NO. 26) (SEQ ID NO. 47) 75-22 DRRSQS RWGDLN  255   (SEQ ID NO. 26) (SEQ ID NO. 48) 75-23 DRRSQS ARDHLN  217   (SEQ ID NO. 26) (SEQ ID NO. 49) 75-24^(a) DRGSQS RSGDLS  166.6 (SEQ ID NO: 5) (SEQ ID NO. 13) 75-25^(a) DRRSQS RSGDLS  267   (SEQ ID NO. 26) (SEQ ID NO. 13) ^(a)beta-alpha orientation of scTv

Example 4: Fab-scTv Fusion Protein Binding to COL6A3-002 and Similar Peptides

Binding affinity of anti-CD3-scTv R4P3F9S fusion proteins towards HLA-A*02 monomers with COL6A3-002 or different similar peptides was measured by biolayer interferometry. Measurements were done on an Octet RED384 system using settings recommended by the manufacturer. Briefly, purified Fab-scTv molecules were loaded onto biosensors (FAB2G) prior to analyzing serial dilutions of HLA-A*02/COL6A3-002. Compared to variants 75-1 and 75-24 comprising wild-type CDRa1 and wild-type CDRb1 increased binding affinities of up to 40-fold were observed for Fab-scTv variants with maturated CDRa1 and/or CDRb1 sequences (Table 3, FIG. 4). In order to evaluate the selectivity of binding to HLA-A*02/COL6A3-002, purified Fab-scTv molecules loaded onto FAB2G biosensors were screened for binding to 1 μM similar peptides (SEQ ID NOs: 28 to 36), each in complex with HLA-A*02. Except of HLA-A*02/COL6A1-001 (SEQ ID NO: 30), which was bound by most of the Fab-scTv variants containing maturated CDRa1 (SEQ ID NO: 26), Fab-scTv variants showed no binding to similar peptides (FIG. 5) arguing for high binding selectivity. For some Fab-scTv variants the therapeutic window between HLA-A*02/COL6A3-002 and HLA-A*02/COL6A1-001 binding was investigated by loading biotinylated peptide-HLA complexes onto biosensors (SA) and analyzing dilution series of Fab-scTv variants. While variant 75-10 comprising maturated CDRa1 (SEQ ID NO: 26) and wild-type CDRb1 (SEQ ID NO: 13) sequence showed 8-fold increased binding affinity to HLA-A*02/COL6A3-002 over HLA-A*02/COL6A1-001, an up to 57-fold increased binding affinity was detected for Fab-scTv variant 75-13 comprising a maturated CDRb1 (SEQ ID NO: 39) arguing for an improvement in therapeutic window (Table 4, FIG. 6).

TABLE 3 Binding affinity of Fab-scTv fusion proteins to HLA-A*02/COL6A3-002. Variant KD (M) kon (1/Ms) koff (1/s) 75-1 8.06E−06 1.01E+05 8.17E−01 75-2 3.69E−06 1.59E+05 5.86E−01 75-3 4.92E−06 9.71E+04 4.78E−01 75-4 5.76E−06 9.78E+04 5.63E−01 75-5 4.32E−04 2.21E+03 9.55E−01 75-6 1.13E−06 2.06E+05 2.32E−01 75-7 1.79E−06 1.93E+05 3.44E−01 75-8 3.45E−06 1.36E+05 4.69E−01 75-9 1.41E−05 6.02E+04 8.51E−01 75-10 1.78E−06 1.69E+05 3.01E−01 75-11 2.82E−07 4.16E+05 1.18E−01 75-12 3.74E−07 2.67E+05 1.00E−01 75-13 4.05E−07 3.28E+05 1.33E−O1 75-14 3.10E−06 8.41E+04 2.61E−01 75-15 7.78E−07 2.33E+05 1.81E−01 75-16 5.87E−07 3.37E+05 1.98E−01 75-17 2.27E−07 3.62E+05 8.20E−02 75-18 1.93E−06 1.51E+05 2.91E−01 75-19 6.00E−07 2.96E+05 1.78E−01 75-20 5.31E−07 6.08E+05 3.23E−01 75-21 5.52E−07 2.72E+05 1.50E−01 75-22 8.22E−07 2.48E+05 2.04E−01 75-23 3.24E−07 3.18E+05 1.03E−01 75-24 5.20E−06 1.08E+05 5.62E−01 75-25 8.33E−06 6.23E+04 5.19E−01

TABLE 4 Comparative binding affinity of Fab-scTv fusion proteins to HLA-A*02/COL6A3-002 and HLA-A*02/COL6A1-001. Variant pHLA-A*02 KD (M) KD_(COL6A1-001)/KD_(COL6A3-002) 75-10 COL6A3-002 1.37E−05 8 COL6A1-001 1.08E−04 75-11 COL6A3-002 8.50E−07 8 COL6A1-001 6.46E−06 75-12 COL6A3-002 7.24E−07 12 COL6A1-001 8.98E−06 75-13 COL6A3-002 7.39E−07 57 COL6A1-001 4.23E−05 75-17 COL6A3-002 8.25E−07 9 COL6A1-001 7.10E−06 75-23 COL6A3-002 1.15E−06 22 COL6A1-001 2.55E−05

Example 5: Use of Affinity-Maturated TCRs for Cellular Expression

Modification of T cells to express TCRs recognizing a tumor-specific peptide-HLA is a promising alternative of redirecting T cells to cancer cells. As the usage of maturated CDR1 sequences could improve cell-bound TCRs against HLA-A*02/COL6A3-002, the identified CDRa1 and CDRb1 mutant sequences were grafted onto the parental TCR R4P3F9 (SEQ ID NOs: 2 and 10). The resulting mutant TCR variants (C-1 to C-18, Table 5) were expressed in human CD8⁺ T cells after electroporation of respective mRNA generated by in vitro transcription of PCR-amplified DNA constructs. For control purpose, the 1G4 TCR (SEQ ID NOs: 53 and 57) against NYESO1-001 peptide (SEQ ID NO: 61) was expressed. After overnight incubation of RNA-electroporated CD8⁺ T cells, expression of introduced TCR variants was analyzed by staining with PE-labeled HLA-A*02/COL6A3-002 tetramers or HLA-A*02/NYESO1-001 tetramers. While the parental TCR R4P3F9 variant C-1 showed only minimal staining with HLA-A*02/COL6A3-002 tetramers, the R4P3F9 TCR variants C-2 to C-18 with maturated CDRa1 and/or CDRb1 showed increased tetramer staining (FIG. 7). Functional activation of CD8⁺ T cells (20,000 cells/well) expressing different maturated R4P3F9 TCR variants was investigated by determining levels of released IFN-gamma upon co-culture with T2 cells (20,000 cells/well) loaded with either a dilution series of COL6A3-002 (SEQ ID NO: 1) or 10 μM of COL6A3-002 and similar peptides (SEQ ID NOs: 28 to 36). Compared to the parental R4P3F9 TCR variant C-1, maturated TCR variants C-2 to C-18 showed increased IFN-gamma release with maximum levels reached already at lower peptide concentrations (FIG. 8). As expected no IFN-gamma release was observed with T cells expressing no TCR or the 1G4 control TCR specific for NYESO1-001. To analyze the selectivity of COL6A3-002 recognition of the maturated R4P3F9 TCR variants, the IFN-gamma release in response to T2 cells loaded with different similar peptides (SEQ ID NOs: 28 to 36) was analyzed and revealed different selectivity profiles for the maturated R4P3F9 TCR variants. Most interestingly, the TCR variants C-5 (SEQ ID Nos 62 and 2) and C-14 (SEQ ID NOs: 62 and 63) comprising the same maturated CDRb1 (SEQ ID NO: 40) did not show any cross-reactivity towards COL6A1-001 or other similar peptides (FIG. 9) making affinity maturated R4P3F9 TCR variants C-5 and C14 most promising candidates for cellular TCR-based tumor targeting.

TABLE 5 Nomenclature of cellular TCR variants. The molecules are based on SEQ ID NOs 2 and 10 and the indicated CDRa1 and CDRb1 variants. Variant CDRa1 CDRb1 C-1 DRGSQS (SEQ ID NO. 5) RSGDLS (SEQ ID NO. 13) C-2 DRGSQS (SEQ ID NO. 5) ARWHNN (SEQ ID NO. 37) C-3 DRGSQS (SEQ ID NO. 5) AKDHLN (SEQ ID NO. 38) C-4 DRGSQS (SEQ ID NO. 5) ARWHRN (SEQ ID NO. 39) C-5 DRGSQS (SEQ ID NO. 5) AMDHPY (SEQ ID NO. 40) C-6 DRGSQS (SEQ ID NO. 5) ATDHYN (SEQ ID NO. 41) C-7 DRGSQS (SEQ ID NO. 5) ARYHTN (SEQ ID NO. 42) C-8 DRGSQS (SEQ ID NO. 5) APYHLN (SEQ ID NO. 43) C-9 DRGSQS (SEQ ID NO. 5) AKDHTN (SEQ ID NO. 44) C-10 DRRSQS (SEQ ID NO. 26) RSGDLS (SEQ ID NO. 13) C-11 DRRSQS (SEQ ID NO. 26) ARWHNN (SEQ ID NO. 37) C-12 DRRSQS (SEQ ID NO. 26) AKDHLN (SEQ ID NO. 38) C-13 DRRSQS (SEQ ID NO. 26) ARWHRN (SEQ ID NO. 39) C-14 DRRSQS (SEQ ID NO. 26) AMDHPY (SEQ ID NO. 40) C-15 DRRSQS (SEQ ID NO. 26) ATDHYN (SEQ ID NO. 41) C-16 DRRSQS (SEQ ID NO. 26) ARYHTN (SEQ ID NO. 42) C-17 DRRSQS (SEQ ID NO. 26) APYHLN (SEQ ID NO. 43) C-18 DRRSQS (SEQ ID NO. 26) AKDHTN (SEQ ID NO. 44)

Example 6: Window of COL6A3-002 and COL6A1-001 Recognition of Cellular TCR Variants

Cellular expression and analysis of R4P3F9 variants was performed as described above. In accordance with previous experiments (FIG. 7), staining of T cells expressing R4P3F9 TCR variants C-2 to C-18 with PE-labeled HLA-A*02/COL6A3-002 tetramers were increased compared to the parental TCR C-1. Additionally, TCR variants C-12 and C-17 showed binding to HLA-A*02/COL6A1-001 (FIG. 10). Expression of all maturated R4P3F9 variants improved functional activation of CD8⁺ T cells in response to T2 cells loaded with a dilution series of COL6A3-002 (SEQ ID NO: 1) reaching 5- to 90-fold lower EC₅₀ values compared to the parental TCR C-1 (FIG. 11, Table 6). The lowest EC₅₀ value was found for variant C-14. Again, TCR variants C-5 (SEQ ID NOs 62 and 2) and C-14 (SEQ ID NOs: 62 and 63) comprising the same maturated CDRb1 (SEQ ID NO: 40) did not show any cross-reactivity towards COL6A1-001, while other variants showed strong recognition with EC₅₀ windows (COL6A3-002 vs. COL6A1-001) as low as factor 5.

TABLE 6 EC₅₀ values [nM] of IFN-γ release of T cells expressing R4P3F9 variants after coculture with T2 cells loaded with COL6A3-002 or COL6A1-001. Variant EC₅₀ COL6A3-002 [nM] EC₅₀ COL6A1-001 [nM] C-1 2.51 — C-2 0.16 — C-3 0.14 871^(a)   C-4 0.13 — C-5 0.15 — C-6 0.48 — C-7 0.29 — C-8 0.20 350    C-9 0.55 — C-10 0.32 1.5 C-11 0.32 8.2 C-12 0.20 1.9 C-13 0.23 9.7 C-14 0.03 — C-15 0.31 69   C-16 0.34 78   C-17 0.33 4.1 C-18 0.14 280089^(a)    ^(a)plateau not reached

Example 7: Efficacy of Maturated R4P3F9 Variants C-5 and C-14 on Tumor Cell Lines

Cellular expression and analysis of R4P3F9 variants was performed as described above.

Expression of the maturated R4P3F9 variants C-5 (SEQ ID NOs 62 and 2) and C-14 (SEQ ID NOs: 62 and 63) improved functional activation of CD8⁺ T cells in response to COL6A3-002 (SEQ ID NO: 1)-presenting tumor cell lines as compared to the parental TCR C-1 (FIG. 12). The tumor cell lines used during this study present different amounts of target peptide. SF539 cells carry ˜4000 copies of HLA-A*02/COL6A3-002 per cell and SW982 cells carry ˜460 copies per cell. Whereas the parental TCR C-1 did not mediate strong T-cell activation upon co-culture with target-positive cell lines, TCR variant C-14 showed even stronger improvement of functional activation than TCR variant C-5. These data are in line with EC₅₀ improvements from TCR C-1 to C-5 and to C-14 (table 6). The target-negative tumor cell line MCF-7 was not recognized by any of these TCRs.

REFERENCES

-   Aleksic et al. 2012: Different affinity windows for virus and     cancer-specific T-cell receptors—implications for therapeutic     strategies, Eur J Immunol. 2012 December; 42(12):3174-9; -   Hickman et al. 2016: Antigen Selection for Enhanced Affinity T-Cell     Receptor-Based Cancer Therapies, J Biomol Screen. 2016 September;     21(8):769-85; -   Boder and Wittrup 2000: Yeast surface display for directed evolution     of protein expression, affinity, and stability, Methods Enzymol.     2000; 328:430-44; -   Boder and Wittrup 1997: Yeast surface display for screening     combinatorial polypeptide libraries, Nat Biotechnol. 1997 June;     15(6):553-7; -   Smith et al. 2015: T Cell Receptor Engineering and Analysis Using     the Yeast Display Platform, Methods Mol Biol. 2015; 1319:95-141; -   DE102016121899.5 -   DE102016115246 

1. A method of treating a patient who has cancer, comprising administering to the patient a population of transformed T cells expressing at least one vector encoding a T cell receptor (TCR), wherein the TCR comprises SEQ ID NOs: 6, 7, 14, and 15, wherein each of SEQ ID NOs: 6, 7, 14, and 15 comprises at most one conservative amino acid substitution, wherein the TCR binds to a peptide consisting of the amino acid sequence of FLLDGSANV (SEQ ID NO: 1) in a complex with an MHC class I molecule, and wherein the cancer is selected from acute lymphocytic cancer, acute myeloid leukemia, alveolar rhabdomyosarcoma, bone cancer, brain cancer, breast cancer, cancer of the anus, anal canal, or anorectum, cancer of the eye, cancer of the intrahepatic bile duct, cancer of the joints, cancer of the neck, gallbladder, or pleura, cancer of the nose, nasal cavity, or middle ear, cancer of the oral cavity, cancer of the vagina, cancer of the vulva, chronic lymphocytic leukemia, chronic myeloid cancer, colon cancer, esophageal cancer, cervical cancer, gastrointestinal carcinoid tumor, glioma, Hodgkin lymphoma, hypopharynx cancer, kidney cancer, larynx cancer, liver cancer, lung cancer, malignant mesothelioma, melanoma, multiple myeloma, nasopharynx cancer, non-Hodgkin lymphoma, cancer of the oropharynx, ovarian cancer, cancer of the penis, pancreatic cancer, peritoneum, omentum, and mesentery cancer, pharynx cancer, prostate cancer, rectal cancer, renal cancer, skin cancer, small intestine cancer, soft tissue cancer, stomach cancer, testicular cancer, thyroid cancer, cancer of the uterus, ureter cancer, gastric cancer, and urinary bladder cancer.
 2. The method of claim 1, wherein the population of transformed cells are produced by a method comprising isolating a T cell from a subject, transforming the cell with at least one vector encoding the TCR to produce a transformed cell, and expanding the transformed cell to produce the population of transformed cells.
 3. The method of claim 2, wherein the subject is the patient.
 4. The method of claim 1, wherein said T cells are CD8+ T cells.
 5. The method of claim 1, wherein the TCR comprises an α chain comprising the amino acid sequence of SEQ ID NO: 2 and a β chain comprising the amino acid sequence of SEQ ID NO: 10, or SEQ ID NO: 22, or SEQ ID NO: 24, or SEQ ID NO: 25, or SEQ ID NO:
 27. 6. The method of claim 1, wherein the MHC class I molecule is HLA-A*02.
 7. The method of claim 1, wherein the population of transformed cells are administered in the form of a pharmaceutical composition.
 8. The method of claim 7, wherein the pharmaceutical composition comprises a chemotherapeutic agent selected from the group consisting of asparaginase, busulfan, carboplatin, cisplatin, daunorubicin, doxorubicin, fluorouracil, gemcitabine, hydroxyurea, methotrexate, paclitaxel, rituximab, vinblastine, and vincristine.
 9. The method of claim 1, wherein the TCR comprises: a CDR1α chain comprising the amino acid sequence of SEQ ID NO: 5 or 26 a CDR2α chain comprising the amino acid sequence of SEQ ID NO: 6, a CDR3α chain comprising the amino acid sequence of SEQ ID NO: 7, a CDR1β chain comprising the amino acid sequence selected from the group consisting of SEQ ID NOs: 13 and 37-44, a CDR2β chain comprising the amino acid sequence of SEQ ID NO: 14, and a CDR3β chain comprising the amino acid sequence of SEQ ID NO: 15, and wherein each of SEQ ID NOs: 5, 26, 13, and 37-44 comprises at most one conservative amino acid substitution.
 10. The method of claim 9, wherein the CDR1α chain comprises the amino acid sequence of SEQ ID NO: 5 and the CDR1β chain comprises the amino acid sequences of SEQ ID NO: 13, wherein each of SEQ ID NOs: 5 and 13 comprises at most one conservative amino acid substitution.
 11. The method of claim 9, wherein the CDR1α chain comprises the amino acid sequence of SEQ ID NO: 5 and the CDR1β chain comprises the amino acid sequences of SEQ ID NO: 37, wherein each of SEQ ID NOs: 5 and 37 comprises at most one conservative amino acid substitution.
 12. The method of claim 9, wherein the CDR1α chain comprises the amino acid sequence of SEQ ID NO: 5 and the CDR1β chain comprises the amino acid sequences of SEQ ID NO: 38, wherein each of SEQ ID NOs: 5 and 38 comprises at most one conservative amino acid substitution.
 13. The method of claim 9, wherein the CDR1α chain comprises the amino acid sequence of SEQ ID NO: 5 and the CDR1β chain comprises the amino acid sequences of SEQ ID NO: 39, wherein each of SEQ ID NOs: 5 and 39 comprises at most one conservative amino acid substitution.
 14. The method of claim 9, wherein the CDR1α chain comprises the amino acid sequence of SEQ ID NO: 5 and the CDR1β chain comprises the amino acid sequences of SEQ ID NO: 40, wherein each of SEQ ID NOs: 5 and 40 comprises at most one conservative amino acid substitution.
 15. The method of claim 9, wherein the CDR1α chain comprises the amino acid sequence of SEQ ID NO: 5 and the CDR1β chain comprises the amino acid sequences of SEQ ID NO: 42, wherein each of SEQ ID NOs: 5 and 42 comprises at most one conservative amino acid substitution.
 16. The method of claim 9, wherein the CDR1α chain comprises the amino acid sequence of SEQ ID NO: 5 and the CDR1β chain comprises the amino acid sequences of SEQ ID NO: 43, wherein each of SEQ ID NOs: 5 and 43 comprises at most one conservative amino acid substitution.
 17. The method of claim 9, wherein the CDR1α chain comprises the amino acid sequence of SEQ ID NO: 26 and the CDR1β chain comprises the amino acid sequences of SEQ ID NO: 38, wherein each of SEQ ID NOs: 26 and 38 comprises at most one conservative amino acid substitution.
 18. The method of claim 9, wherein the CDR1α chain comprises the amino acid sequence of SEQ ID NO: 26 and the CDR1β chain comprises the amino acid sequences of SEQ ID NO: 39, wherein each of SEQ ID NOs: 26 and 39 comprises at most one conservative amino acid substitution.
 19. The method of claim 9, wherein the CDR1α chain comprises the amino acid sequence of SEQ ID NO: 26 and the CDR1β chain comprises the amino acid sequences of SEQ ID NO: 40, wherein each of SEQ ID NOs: 26 and 40 comprises at most one conservative amino acid substitution.
 20. The method of claim 9, wherein the CDR1α chain comprises the amino acid sequence of SEQ ID NO: 26 and the CDR1β chain comprises the amino acid sequences of SEQ ID NO: 44, wherein each of SEQ ID NOs: 26 and 44 comprises at most one conservative amino acid substitution. 